- Trials with a EudraCT protocol (150)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
150 result(s) found for: Rectal pain.
Displaying page 1 of 8.
EudraCT Number: 2014-003351-65 | Sponsor Protocol Number: RDD110 | Start Date*: 2016-03-16 |
Sponsor Name:RDD Pharma Ltd. | ||
Full Title: The Effect of Intra-anal Nifedipine, Used As Add-on to Conservative Therapy, on Pain in Patients with Anal Fissure | ||
Medical condition: Anal Fissure | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BG (Completed) PL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-002632-21 | Sponsor Protocol Number: VRA107438 | Start Date*: 2006-11-13 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development | |||||||||||||
Full Title: A double-blind, randomised, placebo controlled, single dose, two-period crossover study to investigate the therapeutic potential of the TRPV1 antagonist SB-705498 in treatment of subjects with rect... | |||||||||||||
Medical condition: Rectal Hyperalgesia (in patients with irritable bowel syndrome and feacal urgency) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-011753-41 | Sponsor Protocol Number: 0902-127 | Start Date*: 2010-12-23 |
Sponsor Name:Neonatal intensive care unit, VU medical center Amsterdam | ||
Full Title: Pain treatment of newborns: paracetamol rectal versus intraveneous administration, an open randomised clinical trial. | ||
Medical condition: Pain treatment of neonates and premature neonates. | ||
Disease: | ||
Population Age: Preterm newborn infants, Newborns, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2006-006855-10 | Sponsor Protocol Number: RXQ229 | Start Date*: 2007-02-23 |
Sponsor Name:Buckinghamshire Hospitals NHS Trust | ||
Full Title: A randomised trial of rectal stimulants for neurogenic bowel management after spinal cord injury | ||
Medical condition: Response of the neurogenic bowel after spinal cord injury to pharmacological rectal stimulants | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2010-023938-23 | Sponsor Protocol Number: Antrorect/02/09 | Start Date*: 2011-01-12 | |||||||||||
Sponsor Name:BRACCO | |||||||||||||
Full Title: Effect of Mesalazine plus nifedipine suppositoires (Antrorect) in functional ano-rectal pain disorders: a pilot randomized double-blind placebo-controlled study. | |||||||||||||
Medical condition: Functional ano-rectal pain disorders | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004916-21 | Sponsor Protocol Number: EROS | Start Date*: 2019-07-02 | |||||||||||
Sponsor Name:Karolinska Institute | |||||||||||||
Full Title: Early intervention and recovery of sexual function in men and women after treatment of rectal cancer–a randomized controlled study with tadalafil compared to standard care | |||||||||||||
Medical condition: sexual/ erectile function in women and men after treatment for rectal cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-004166-33 | Sponsor Protocol Number: LARC_Deep_Cancer | Start Date*: 2019-04-17 |
Sponsor Name:ISTITUTO NAZIONALE TUMORI - IRCCS FONDAZIONE PASCALE | ||
Full Title: ORGAN SPARING FOR LOCALLY ADVANCED RECTAL CANCER AFTER NEOADJUVANT TREATMENT FOLLOWED BY ELECTROCHEMOTHERAPY | ||
Medical condition: locally advanced rectal cancer | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: IT (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2006-004578-29 | Sponsor Protocol Number: P.sitsen.01 | Start Date*: 2007-06-15 |
Sponsor Name:Leids Universitair Medisch Centrum | ||
Full Title: The efficacy of intravenous versus rectal paracetamol: A randomized, prospective, double-blind placebo-controlled study | ||
Medical condition: Aims of the study 1)to compare the analgesic efficacy of intravenous versus rectal paracetamol versus placebo as assessed by VAS scores and PCA morphine consumption. 2)To assess the pharmacokinet... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2016-000135-40 | Sponsor Protocol Number: 260585 | Start Date*: 2016-05-12 | ||||||||||||||||||||||||||
Sponsor Name:Zealand University Hospital, Department of Surgery | ||||||||||||||||||||||||||||
Full Title: Endoscopic assisted electrochemotherapy in addition to neoadjuvant treatment of locally advanced rectal cancer: a randomized clinical phase II trial. | ||||||||||||||||||||||||||||
Medical condition: Locally advanced rectal cancer | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-002882-19 | Sponsor Protocol Number: MCHT001 | Start Date*: 2004-12-10 |
Sponsor Name:Mid Cheshire Hospitals NHS Trust | ||
Full Title: A controlled trial into the benefit of topical perianal glyceryl trinitrate (GTN) as a sphincter relaxant, pre-insertion of ultrasound probe for trans rectal ultrasound (TRUS) guided biopsy of the ... | ||
Medical condition: Prostate Cancer Diagnosis – Pain relief during biopsy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2004-000383-27 | Sponsor Protocol Number: D1803C00002 | Start Date*: 2004-07-28 |
Sponsor Name:AstraZeneca AB | ||
Full Title: A double-blind randomized placebo controlled crossover study of AZD7371 ER 5 mg bid, 20 mg bid and placebo treatment for one week on visceral perception and symptoms in patients with Irritable Bowe... | ||
Medical condition: Irritable Bowel Syndrome (IBS) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-004578-25 | Sponsor Protocol Number: AUCH-1 | Start Date*: 2021-07-09 |
Sponsor Name:BioGaia Pharma AB | ||
Full Title: A randomised placebo-controlled safety study of Lactobacillus reuteri BGP-014 in patients with active mild to moderate ulcerative colitis | ||
Medical condition: Mild to moderate ulcerative colitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-004844-37 | Sponsor Protocol Number: ACG-CR-065-2013 | Start Date*: 2015-07-16 |
Sponsor Name:Enrique de Madaria Pascual | ||
Full Title: A Randomized Controlled Pilot Trial of Indomethacin in Acute Pancreatitis | ||
Medical condition: Acute pancreatitis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2007-004526-24 | Sponsor Protocol Number: Panbio/CR/0042006/CT | Start Date*: 2008-09-23 | |||||||||||
Sponsor Name:Panacea Biotec Ltd | |||||||||||||
Full Title: A double-blind, randomized, placebo-controlled, multicentre study to assess the efficacy and safety of Euphorbia Prostrata Dry Extract Tablets in patients of 1° and 2° internal haemorrhoids | |||||||||||||
Medical condition: Male and female subjects, at least 18 years of age with a diagnosis of internal haemorrhoids (1° and 2°) confirmed by protoscopic examination and suffering form an uncomplicated and untreated acute... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-006283-42 | Sponsor Protocol Number: KAD166 | Start Date*: 2012-04-30 | |||||||||||
Sponsor Name:Dr. Kade Pharmazeutische Fabrik GmbH | |||||||||||||
Full Title: Placebo-controlled double-blind trial investigating the efficacy and tolerability of Posterisan® akut with lidocaine (50 mg/g rectal ointment) in abatement of complaints associated with the anorect... | |||||||||||||
Medical condition: Relief of complaints associated with anorectal symptom complex (pain, burning, itching) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003466-25 | Sponsor Protocol Number: 13.024 | Start Date*: 2014-12-18 | |||||||||||
Sponsor Name:Anders Gadegaard Jensen,Anesthesia and Intensive Care Unit, Odense University Hospital | |||||||||||||
Full Title: Randomized, double-blind, prospective, placebo-controlled trial of the effect of intravenous lidocaine infusion for postoperative pain management and bowel function in robot assisted laparoscopic c... | |||||||||||||
Medical condition: Postoperative pain after colon rectal cancer surgery are mainly intended to relieve as well resting as activity-induced pain. Secondarily, the choice of pain management should take into considerati... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003048-11 | Sponsor Protocol Number: GIPIT002 | Start Date*: 2014-10-24 |
Sponsor Name:GIPIT | ||
Full Title: FEcal transplant, a Dazzling debut to Eradicate colonization with eXtreme drug resistant bacteria? | ||
Medical condition: Patient harboring Extreme Drug Resistant (XDR) bacteria. Our trial try to eradicate this digestive tract colonization by performing a fecal transplantation. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2004-004077-29 | Sponsor Protocol Number: 2004112 | Start Date*: 2005-02-04 |
Sponsor Name:Procter & Gamble Pharmaceuticals | ||
Full Title: A Double-blind, Randomized, Multicenter, Active-control, 56-day Study with a 28-day Follow-up to Assess the Efficacy and Safety of RDP58 200 mg/day plus Mesalazine 2.4 g/day and RDP58 600 mg/day pl... | ||
Medical condition: Ulcerative colitis is characterized by acute and chronic inflammatory changes to the mucosa and submucosa of the colon and rectum. Clinical presentations include increased stool frequency, bloody d... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) LT (Completed) SK (Completed) CZ (Completed) GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-001069-17 | Sponsor Protocol Number: CSPI135ZDE04 | Start Date*: 2004-09-16 | |||||||||||
Sponsor Name:Novartis Pharma GmbH | |||||||||||||
Full Title: A double-blind, active-controlled, randomized, multicenter, parallel-group 2 day comparison of 1000 mg propyphenazone / 80 mg codeine (applied as two suppositories) combination therapy versus a 100... | |||||||||||||
Medical condition: acute, at least moderate to severe biliary or urogenital pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-002012-27 | Sponsor Protocol Number: KEDOB | Start Date*: 2013-10-30 |
Sponsor Name:LANDSTINGET I ÖSTERGÖTLAND | ||
Full Title: Ketamine dose finding study in pediatric burn wound care | ||
Medical condition: Pediatric burn patients who need rectal sedation during wound care | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
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