- Trials with a EudraCT protocol (107)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
107 result(s) found for: Oxytocin.
Displaying page 3 of 6.
EudraCT Number: 2015-004463-37 | Sponsor Protocol Number: 140682 | Start Date*: 2016-06-20 |
Sponsor Name:St. Olavs Hospital | ||
Full Title: ACUTE AND LONG-TERM EFFECTS OF INTRANASAL OXYTOCIN IN ALCOHOL WITHDRAWAL AND DEPENDENCE: A PROSPECTIVE RANDOMIZED PARALLEL GROUP PLACEBO-CONTROLLED TRIAL | ||
Medical condition: alcohol withdrawal and craving. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NO (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-004325-16 | Sponsor Protocol Number: RC31/16/8407 | Start Date*: 2016-12-22 |
Sponsor Name:University Hospital of Toulouse | ||
Full Title: Long term evaluation of infants aged from 3 to 4 years old included in the OTBB2 study (repeated administrations of oxytocin in infants with PWS aged from 0 to 6 months) and comparison with not tre... | ||
Medical condition: Prader Willi Syndrom | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-001346-92 | Sponsor Protocol Number: Nitroglycerin2 | Start Date*: 2008-05-23 |
Sponsor Name:No sponsor | ||
Full Title: Medical treatment with nitroglycerin for management of retained placenta - a multicentre trial | ||
Medical condition: Background: retained placenta occurs in 3% of all deliveries. The results from a pilot study indicate that medical treatment with a combination of oxytocin and the utero-relaxing agent nitroglycer... | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-000769-35 | Sponsor Protocol Number: S61358 | Start Date*: 2018-09-27 | |||||||||||
Sponsor Name:University Hospital, KU Leuven | |||||||||||||
Full Title: In search for an innovative neural marker and intervention for socio-communicative difficulties in children with and without autism spectrum disorders | |||||||||||||
Medical condition: Autism Spectrum Disorders | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004224-10 | Sponsor Protocol Number: N/A | Start Date*: 2013-12-06 |
Sponsor Name:Region Skåne | ||
Full Title: Prospective randomized trial comparing the effects of oxytocin and carbetocin on circulation and vascular tone at cesarean section | ||
Medical condition: Cesarean section of pregnant women | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2022-003670-22 | Sponsor Protocol Number: IIBSP-OXI-2022-124 | Start Date*: 2023-07-31 |
Sponsor Name:Institut de Recerca Hospital de la Santa Creu i Sant Pau - IIB Sant Pau | ||
Full Title: Controlled and randomized clinical trial to evaluate the efficacy of the combination of oxytocin plus self-compassion training in patients with Borderline Personality Disorder | ||
Medical condition: Borderline personality disorder | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-003423-30 | Sponsor Protocol Number: 2017-RCT-OX | Start Date*: 2017-12-12 | |||||||||||
Sponsor Name:Dutch Growth Research Foundation | |||||||||||||
Full Title: Randomized, double-blind, placebo-controlled oxytocin and dose-response trial in children with Prader-Willi syndrome. Effects on social behaviour. | |||||||||||||
Medical condition: Prader-Willi syndrome | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-003072-39 | Sponsor Protocol Number: 41223 | Start Date*: 2012-11-27 | |||||||||||
Sponsor Name:Academic Medical Center, University of Amsterdam | |||||||||||||
Full Title: Oxytocin in PTSD: effectiveness as addition to Narrative Exposure Therapy | |||||||||||||
Medical condition: Posttraumatic stress disorder | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000029-29 | Sponsor Protocol Number: P/2013/160 | Start Date*: 2013-08-30 |
Sponsor Name:Centre Hospitalier Régional Universitaire de Besancon | ||
Full Title: Study of the effect of oxytocin on emotion regulation in adolescents with insecure attachment | ||
Medical condition: | ||
Disease: | ||
Population Age: Adolescents, Under 18 | Gender: Male | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-002338-19 | Sponsor Protocol Number: BUSCLAB001 | Start Date*: 2019-01-22 |
Sponsor Name:Oslo University Hospital | ||
Full Title: BUSCLAB - A DOUBLE BLIND RANDOMIZED PLACEBO-CONTROLLED TRIAL INVESTIGATING THE EFFECT OF INTRAVENOUS BUTYLSCOPOLAMINE BROMIDE TO TREAT SLOW PROGRESS IN LABOR | ||
Medical condition: To study the effect of Butylscopolamide Bromide on duration of the active phase of first stage of labor in women who cross the alert-line for labor dystocia, according to the WHO partograph. | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NO (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-005465-20 | Sponsor Protocol Number: OXYPEP002 | Start Date*: 2012-01-27 | |||||||||||
Sponsor Name:PeP-Tronic Medical AB | |||||||||||||
Full Title: A double-blind, placebo controlled single centre trial to evaluate the dose-relationship of the effects of vaginally administered oxytocin on the vaginal mucosal membrane in postmenopausal women | |||||||||||||
Medical condition: Vaginal atrophy in postmenopausal women | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022511-18 | Sponsor Protocol Number: X04 | Start Date*: 2011-04-05 | |||||||||||
Sponsor Name:Albert-Ludwig University Freiburg, Laboratory for Biological and Personality Psychology | |||||||||||||
Full Title: Behavioral effects and neural correlates of oxytocin on social attention [Verhaltenseffekte und neuronales Korrelat von Oxytocin im Kontext sozialer Aufmerksamkeit] | |||||||||||||
Medical condition: subjects with autism spectrum disorder and neurotypical controls | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-001310-34 | Sponsor Protocol Number: OXY-COUP-PROT1.4 | Start Date*: 2011-08-11 |
Sponsor Name:Med. Univ. Wien, Univ. Klinik für Innere Med. III | ||
Full Title: Female Sexual Dysfunction in the Peri and Postmenopause: Effect of intranasal Oxytocin administration on sexual function and activity | ||
Medical condition: Sexual behaviour with reduced intercourse frequency due to female sexual function disorders | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-002949-20 | Sponsor Protocol Number: LWH0747 | Start Date*: 2008-04-28 | |||||||||||
Sponsor Name:Liverpool Women's NHS Foundation Trust | |||||||||||||
Full Title: Randomised controlled trial comparing the effects of oxytocin 5 units IV bolus vs oxytocin 5 units IV infusion on cardiac output during caesarean section | |||||||||||||
Medical condition: The drug is given routinely to women during caesarean section to help the womb contract after their baby has been delivered. This helps reduce the risk of bleeding after surgery. For this trial, ... | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-002942-30 | Sponsor Protocol Number: 01012015 | Start Date*: 2015-12-10 | ||||||||||||||||
Sponsor Name:Regional Hospital of Randers | ||||||||||||||||||
Full Title: CONDISOX: Continued versus discontinued oxytocin stimulation of labour in a double-blind randomised controlled trial | ||||||||||||||||||
Medical condition: Syntocinon is used for labour induction to stimulate contractions. The current recommendation is to stimulate until delivery. We hypothesize that discontinuation of Syntocinon when the active phase... | ||||||||||||||||||
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Population Age: Adults | Gender: Female | |||||||||||||||||
Trial protocol: DK (Completed) NL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-002385-12 | Sponsor Protocol Number: RC31/15/7825 | Start Date*: 2019-08-27 |
Sponsor Name:University Hospital of Toulouse | ||
Full Title: OXYTOCIN TREATMENT IN NEONATES AND INFANTS AGED FROM 0 TO 3 MONTHS WITH PRADER-WILLI SYNDROME: A STUDY OF THE SAFETY AND EFFICACY ON ORAL AND SOCIAL SKILLS AND, FEEDING BEHAVIOR OF INTRANASAL ADMIN... | ||
Medical condition: Prader-Willi Syndrom | ||
Disease: | ||
Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: FR (Completed) BE (Completed) NL (Prematurely Ended) DE (Completed) IT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-000158-36 | Sponsor Protocol Number: OXYPEP202 | Start Date*: 2016-03-18 | |||||||||||
Sponsor Name:PEPTONIC medical AB | |||||||||||||
Full Title: A Phase 2b, Double-blind, Randomized, Parallel, Placebo-Controlled Study to Evaluate the 12-week Efficacy of Vagitocin in Postmenopausal Women with Symptoms of Vulvovaginal Atrophy | |||||||||||||
Medical condition: Vaginal Atrophy | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-000989-15 | Sponsor Protocol Number: DR200090 | Start Date*: 2021-07-28 | |||||||||||
Sponsor Name:University Hospital, Tours | |||||||||||||
Full Title: Oxytocin versus Prostaglandins for labor Induction of women with an unfavorable Cervix after 24 hours of cervical ripening: a multicenter non inferiority randomized trial | |||||||||||||
Medical condition: Labor Induction of women with an unfavorable Cervix after 24 hours of cervical ripening | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-003273-18 | Sponsor Protocol Number: RC31-15-7837 | Start Date*: 2016-11-14 |
Sponsor Name:University Hospital of Toulouse | ||
Full Title: Effects of intranasal administrations of oxytocin on beahvioural troubles, hyperphagia and social skills in children with Prader-Willi syndrome aged from 3 to 12 years. | ||
Medical condition: Prader-Willi Syndrom | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-005431-13 | Sponsor Protocol Number: OTMother2015 | Start Date*: 2015-01-13 |
Sponsor Name:Tampere University Hospital | ||
Full Title: Effects of maternal oxytocin on social information processing in mothers and infants | ||
Medical condition: There are no medical conditions or diseases under investigation, participants are healthy volunteers. | ||
Disease: | ||
Population Age: Infants and toddlers, Under 18, Adults | Gender: Female | |
Trial protocol: FI (Completed) | ||
Trial results: (No results available) |
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