- Trials with a EudraCT protocol (53)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
53 result(s) found for: Endometriosis AND Pain.
Displaying page 1 of 3.
EudraCT Number: 2022-002424-12 | Sponsor Protocol Number: KETA-TEAM | Start Date*: 2022-11-17 | |||||||||||
Sponsor Name:Médipôle Hôpital Mutualiste | |||||||||||||
Full Title: KETA-TEAM A Phase 2 Study to Assess the Safety and Efficacy of Ketamine, Treatment for Endometriosis-related chronic pain as Analgesic in Médipôle | |||||||||||||
Medical condition: Endometriosis with refractory chronic pelvic pain | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-008722-73 | Sponsor Protocol Number: PPP/2008 | Start Date*: 2009-04-20 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA PISANA | |||||||||||||
Full Title: ROLE OF PAROXETINE AS ADD-ON THERAPY TO GNRH AGONIST IN THE TREATMENT OF ENDOMETRIOSIS-RELATED CHRONIC PELVIC PAIN | |||||||||||||
Medical condition: Endometriosis-associated pelvic pain | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-001810-21 | Sponsor Protocol Number: 2022-001810-21 | Start Date*: 2022-08-23 | |||||||||||
Sponsor Name:Aarhus University Hospital, Department of Anaesthesiology | |||||||||||||
Full Title: Intraoperative clonidine for postoperative pain management in patients undergoing surgical treatment for endometriosis: a prospective, double-blind, randomized controlled trial | |||||||||||||
Medical condition: Endometriosis | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005744-17 | Sponsor Protocol Number: ENDOMET-IA-DIULNG08 | Start Date*: 2008-11-10 | |||||||||||||||||||||||||||||||
Sponsor Name:PEDRO ACIEN ALVAREZ | |||||||||||||||||||||||||||||||||
Full Title: INHIBIDORES DE LA AROMATASA (ANASTROZOL) ASOCIADOS A DISPOSITIVO INTRAUTERINO LIBERADOR DE LEVONORGESTREL (DIU-LNG) EN EL TRATAMIENTO DE LA ENDOMETRIOSIS MODERADA/SEVERA | |||||||||||||||||||||||||||||||||
Medical condition: ENDOMETRIOSIS MODERADA/SEVERA | |||||||||||||||||||||||||||||||||
|
|||||||||||||||||||||||||||||||||
Population Age: Adults | Gender: Female | ||||||||||||||||||||||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-017169-53 | Sponsor Protocol Number: BAY86-5258/13788 | Start Date*: 2011-01-17 | |||||||||||
Sponsor Name:Bayer HelathCare AG | |||||||||||||
Full Title: Estudio multicéntrico, abierto, de un brazo de tratamiento para evaluar la seguridad y la eficacia de la administración oral diaria de 2 mg de Dienogest en el tratamiento de la endometriosis en ado... | |||||||||||||
Medical condition: Sospecha clínica o confirmada de endometriosis en mujeres adolescentes post-menarquia de 12 a menos de 18 años de edad (Clinically suspected or confirmed endometriosis in post menarche female adole... | |||||||||||||
|
|||||||||||||
Population Age: Adolescents, Under 18 | Gender: Female | ||||||||||||
Trial protocol: ES (Completed) FI (Completed) DE (Completed) AT (Completed) FR (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-000993-32 | Sponsor Protocol Number: S55300 | Start Date*: 2013-05-07 | ||||||||||||||||
Sponsor Name:University Hospital Leuven | ||||||||||||||||||
Full Title: Does prolonged GnRH downregulation prior to ART improve the clinical pregnancy rate in postoperative endometriosis patients? A RCT | ||||||||||||||||||
Medical condition: endometriosis, subfertility | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults | Gender: Female | |||||||||||||||||
Trial protocol: BE (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-000244-18 | Sponsor Protocol Number: BAY1128688/17472 | Start Date*: 2017-09-25 | ||||||||||||||||
Sponsor Name:Bayer AG | ||||||||||||||||||
Full Title: A randomized, placebo-controlled, double-blind, parallel-group, multi-center, exploratory dose-response study to assess the efficacy and safety of different oral doses of BAY 1128688 in women with ... | ||||||||||||||||||
Medical condition: Endometriosis | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults | Gender: Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) ES (Prematurely Ended) HU (Prematurely Ended) FI (Prematurely Ended) CZ (Prematurely Ended) AT (Prematurely Ended) DE (Prematurely Ended) BE (Prematurely Ended) DK (Prematurely Ended) NL (Prematurely Ended) PL (Prematurely Ended) IT (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-005167-24 | Sponsor Protocol Number: PGL11-007 | Start Date*: 2012-05-04 | |||||||||||
Sponsor Name:PregLem S.A. | |||||||||||||
Full Title: A Phase II, Multicentre, Randomised, Two-Arm, Parallel Group, Double-Blind, Placebo controlled Study of the Steroid Sulfatase Inhibitor PGL2001 with concomitant administration of NETA (norethistero... | |||||||||||||
Medical condition: Treatment of symptoms related to endometriosis | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: HU (Completed) PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-005494-53 | Sponsor Protocol Number: | Start Date*: 2014-10-16 | |||||||||||||||||||||||||||||||
Sponsor Name:Norfolk and Norwich University Hospitals NHS Foundation Trust | |||||||||||||||||||||||||||||||||
Full Title: A Study of the Histopathological Changes within Ectopic Endometrial Tissue, in Subjects with Known Pelvic Endometriosis Following Treatment with Ulipristal Acetate, a Selective Progesterone Recepto... | |||||||||||||||||||||||||||||||||
Medical condition: Endometriosis | |||||||||||||||||||||||||||||||||
|
|||||||||||||||||||||||||||||||||
Population Age: Adults | Gender: Female | ||||||||||||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-004768-72 | Sponsor Protocol Number: BAY1002670/15792 | Start Date*: 2018-06-11 | |||||||||||
Sponsor Name:Bayer AG | |||||||||||||
Full Title: A randomized, double-blind, parallel-group, multicenter Phase 2b study to assess the efficacy and safety of two different doses of vilaprisan (BAY 1002670) versus placebo in women with symptomatic ... | |||||||||||||
Medical condition: Pre-menopausal women 18 years and older with confirmed endometriosis and moderate to severe endometriosis-associated pelvic pain (EAPP), otherwise in good general health. | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: AT (Completed) FI (Completed) DK (Prematurely Ended) SE (Prematurely Ended) ES (Prematurely Ended) DE (Prematurely Ended) HU (Completed) BG (Prematurely Ended) CZ (Prematurely Ended) PL (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-004752-21 | Sponsor Protocol Number: ISI-06-01 | Start Date*: 2006-11-08 | |||||||||||
Sponsor Name:Karolinska Institute, Danderyds hospital | |||||||||||||
Full Title: Pertubation with Lignocaine in Endometriosis Associated Symptoms Effect study (PLEASE) | |||||||||||||
Medical condition: Women 20-40 years of age with endometriosis and pelvic pain will be included in this study. | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-001736-35 | Sponsor Protocol Number: 15-OBE2109-001 | Start Date*: 2016-08-29 | |||||||||||||||||||||
Sponsor Name:ObsEva SA | |||||||||||||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, phase 2b dose-ranging study to assess the efficacy and safety of OBE2109 in subjects with endometriosis associated pain. | |||||||||||||||||||||||
Medical condition: Treatment of Endometriosis-Associated Pain | |||||||||||||||||||||||
|
|||||||||||||||||||||||
Population Age: Adults | Gender: Female | ||||||||||||||||||||||
Trial protocol: PL (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-001984-21 | Sponsor Protocol Number: 3/013/13 | Start Date*: 2013-09-11 | |||||||||||
Sponsor Name:University of Aberdeen & NHS Grampian | |||||||||||||
Full Title: PRE-EMPT: Preventing Recurrence of Endometriosis by Means of long acting Protestogen Therapy | |||||||||||||
Medical condition: Endometriosis | |||||||||||||
|
|||||||||||||
Population Age: Adolescents, Under 18, Adults | Gender: Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-003829-28 | Sponsor Protocol Number: TAK-013/EC204 | Start Date*: 2004-12-22 | |||||||||||
Sponsor Name:Takeda Europe R&D Centre Ltd | |||||||||||||
Full Title: An open-label investigation into the tolerability and pharmacokinetic / pharmacodynamic effects of sufugolix (TAK-013), at a dosage of 100mg twice-daily, during six months treatment of pre-menopaus... | |||||||||||||
Medical condition: symptomatic endometriosis | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-001721-13 | Sponsor Protocol Number: TAK-013/EC-302 | Start Date*: 2005-01-24 | |||||||||||
Sponsor Name:Takeda Europe R&D Center Ltd | |||||||||||||
Full Title: A Phase III, multi-center, randomized, double-blind study to evaluate the efficacy and safety of 50 mg and 100 mg of sufugolix (TAK-013) tablets administered twice daily versus placebo for 12 weeks... | |||||||||||||
Medical condition: Endometriosis | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001219-22 | Sponsor Protocol Number: PGL11-021 | Start Date*: 2012-06-11 | ||||||||||||||||
Sponsor Name:PregLem S.A. | ||||||||||||||||||
Full Title: A Phase IIa study investigating the efficacy and safety of the c-Jun-N-Terminal Kinase (JNK) inhibitor PGL5001 versus placebo administered for up to 5 months with concomitant administration of depo... | ||||||||||||||||||
Medical condition: Peritoneal and/or ovarian endometriosis with an inflammatory component. | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults | Gender: Female | |||||||||||||||||
Trial protocol: PL (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001720-21 | Sponsor Protocol Number: TAK-013/EC301 | Start Date*: 2004-12-24 | |||||||||||
Sponsor Name:Takeda Europe R&D Centre Ltd | |||||||||||||
Full Title: A Phase III, multi-center, randomized, double-blind comparator study to evaluate the efficacy and safety of 50 mg and 100 mg of TAK-013 tablets administered twice daily versus 3.75mg of Leuprolide ... | |||||||||||||
Medical condition: Endometriosis | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000915-26 | Sponsor Protocol Number: 000295 | Start Date*: 2019-05-10 | |||||||||||
Sponsor Name:Ferring Pharmaceuticals A/S | |||||||||||||
Full Title: A randomised, double-blind, placebo-controlled, proof-of-mechanism phase 2 trial investigating the effect of quinagolide extended-release vaginal ring on reduction of lesions assessed by high-resol... | |||||||||||||
Medical condition: Deep infiltrating endometriosis, endometrioma and/or adenomyosis. | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) DK (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-004302-63 | Sponsor Protocol Number: CLI20001/Lita005 | Start Date*: 2020-12-15 | |||||||||||
Sponsor Name:Litaphar Laboratorios S.L. | |||||||||||||
Full Title: A multi-centre, open-label, single-arm study assessing the safety and efficacy of 5 mg of mifepristone for the treatment of endometriosis in reproductive-age women during two treatment cycles of 24... | |||||||||||||
Medical condition: endometriosis in reproductive-age | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: HU (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-003131-16 | Sponsor Protocol Number: 20584 | Start Date*: 2021-01-25 | |||||||||||
Sponsor Name:Bayer AG | |||||||||||||
Full Title: A randomized, double-blind, open for active comparator, parallel-group, multicenter Phase 2b study to assess the efficacy and safety of three different doses of P2X3 antagonist (BAY 1817080) versus... | |||||||||||||
Medical condition: Treatment of pain related to endometriosis | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) CZ (Completed) SK (Completed) FI (Completed) NO (Completed) AT (Completed) LT (Completed) PL (Completed) BE (Completed) BG (Prematurely Ended) HU (Completed) GR (Completed) EE (Completed) LV (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
Subscribe to this Search
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
To subscribe to the RSS feed for this search click here

Download Options: | |
---|---|
Number of Trials to download: | |
Download Content: | |
Download Format: | |
Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial. |
