- Trials with a EudraCT protocol (26)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
26 result(s) found for: Roux-en-Y.
Displaying page 1 of 2.
EudraCT Number: 2014-002323-10 | Sponsor Protocol Number: absorptiontrial | Start Date*: 2014-07-21 |
Sponsor Name:Rijnstate | ||
Full Title: Iron absorptiontrail after Roux- en -Y Gastric Bypass | ||
Medical condition: Patients who are eligible for a primary Roux- en -Y gastric bypass and who have no irondificiency | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-002260-10 | Sponsor Protocol Number: MCL-metoprolol-IR | Start Date*: 2013-07-11 |
Sponsor Name:Medisch Centrum Leeuwarden | ||
Full Title: The effect of Roux-en-Y gastric bypass on the rate and extent of absorption of metoprolol from an immediate release tablet in female bariatric patient volunteers: a single oral dose study before an... | ||
Medical condition: Roux-en-Y gastric bypass | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2012-005387-10 | Sponsor Protocol Number: ERY-PAO | Start Date*: 2013-03-27 |
Sponsor Name:Department of hospital Pharmacy, Medical Centre Haaglanden | ||
Full Title: Effect of Roux-en-Y gstric bypass surgery in morbidly obese patients on Pharmacokinetics of (Acetyl)salicylic acid and Omeprazole. | ||
Medical condition: Roux-en-Y gastric bypass (RYGB) surgery is a successful treatment for morbid obesity. In this procedure, a small gastric pouch is created. The duodenum is bypassed by connecting the jejunum to this... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-002274-41 | Sponsor Protocol Number: MCL-metoprolol-CR | Start Date*: 2013-07-11 |
Sponsor Name:Medisch Centrum Leeuwaarden | ||
Full Title: The effect of Roux-en-Y gastric bypass on the rate and extent of absorption of metoprolol from a controlled release tablet in female bariatric patient volunteers: a single oral dose study before an... | ||
Medical condition: Roux-en-Y gastric bypass | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-005006-62 | Sponsor Protocol Number: ASZ-001 | Start Date*: 2019-12-10 | |||||||||||
Sponsor Name:Albert Schweitzer hospital | |||||||||||||
Full Title: Pharmacokinetics of Paracetamol before and after Roux-en-Y gastric bypass | |||||||||||||
Medical condition: Roux-en-Y gastric bypass | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001143-40 | Sponsor Protocol Number: OBEMO1EXT | Start Date*: 2016-06-22 |
Sponsor Name:Therapeutic Research Unit | ||
Full Title: Long-term effects of Roux-en-Y Gastric Bypass on morphine exposure after oral administration of immediate release morphine, in comparison with subjects without surgery | ||
Medical condition: Subjects volunteers who undergone Roux-en-Y gastric bypass (RYGB) for at least 48 months and control subjects matched for BMI, age and sex | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2014-002322-12 | Sponsor Protocol Number: Ironsuppletiontrial | Start Date*: 2014-07-24 |
Sponsor Name:Rijnstate Hospital | ||
Full Title: Optimizing Iron suppletion trial after Roux- en -Y Gastric Bypass | ||
Medical condition: Patients who underwent a gastric bypass and develop an irondeficiency postoperatively. The medical condition which is investigated is irondeficiency | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2016-003245-29 | Sponsor Protocol Number: SA652013 | Start Date*: 2016-12-19 |
Sponsor Name:Amsterdam AMC, locatie AMC | ||
Full Title: Ursodeoxycholic acid for the prevention of symptomatic gallstone disease after Roux-en-Y gastric bypass and Sleeve Gastrectomy | ||
Medical condition: Prevention of symptomatic gallstone disease | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-001444-37 | Sponsor Protocol Number: Irontrial | Start Date*: 2014-07-21 |
Sponsor Name:Rijnstate Hospital | ||
Full Title: Optimizing iron suppletion after Roux-en-Y Gastric Bypass | ||
Medical condition: Patients who underwent a gastric bypass and develop a irondeficiency postoperatively. The medical condition which is investigated is irondeficiency | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2012-001244-22 | Sponsor Protocol Number: INOGMA-PK1 | Start Date*: 2012-07-16 |
Sponsor Name:KU Leuven - Centre for Pharmacotherapy | ||
Full Title: Influence of obesity and gastric bypass on medication absorption: pharmacokinetic study | ||
Medical condition: Obese volunteers and volunteers with a Roux-en-Y gastric bypass (RYGB) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2022-000178-24 | Sponsor Protocol Number: W2021.040 | Start Date*: 2023-10-20 |
Sponsor Name: | ||
Full Title: Active vitamin D for secondary hyperparathyroidism after bariatric surgery: a multicenter randomized controlled trial. | ||
Medical condition: patients with secondary hyperparathyroidism after Roux-en-Y gastric bypass surgery (RYGB). | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2013-004835-60 | Sponsor Protocol Number: VITAAL2 | Start Date*: 2014-06-05 |
Sponsor Name:Rijnstate Hospital | ||
Full Title: Vitamin Deficiencies and Supplementation in Morbidly obese | ||
Medical condition: Vitamin B12 deficiencies | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-001086-50 | Sponsor Protocol Number: HypoGB2015 | Start Date*: 2015-06-03 | |||||||||||
Sponsor Name:Køge Sygehus | |||||||||||||
Full Title: Treatment of hypoglycemia following gastric bypass surgery | |||||||||||||
Medical condition: Postprandial reactive hypoglycemia in patients with prior Roux-en-Y gastric bypass surgery. | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002816-19 | Sponsor Protocol Number: Frax001 | Start Date*: 2012-10-25 |
Sponsor Name:Rijnstate Hospital | ||
Full Title: Prospective, pharmacokinetic study for determination of the relationship between lean body weight and anti-Xa activity 4 hours after subcutaneous injection of 5700 IU nadroparin in morbidly obese p... | ||
Medical condition: patients; perioperative in bariatric surgery | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2004-005012-80 | Sponsor Protocol Number: S245.4007 | Start Date*: 2005-03-03 |
Sponsor Name:Solvay Pharmaceuticals GmbH | ||
Full Title: Double-blind, multicenter, randomized, placebo-controlled, parallel-group study to investigate the effect of Creon 25 000 Minimicrospheres on body mass index (BMI) in patients after gastrectomy. | ||
Medical condition: Patients atleast 18 years old with total or subtotal gastrektomy. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-001677-15 | Sponsor Protocol Number: 08/H0808/2 | Start Date*: 2008-07-21 | |||||||||||
Sponsor Name:King's College Hospital NHS Foundation Trust | |||||||||||||
Full Title: The effect of intraoperative N-acetylcysteine on hepatocellular injury during laparoscopic bariatric surgery. A randomised controlled trial. | |||||||||||||
Medical condition: Non-Alcoholic Fatty Liver Disease in patients undergoing weight-loss (bariatric) surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-000548-71 | Sponsor Protocol Number: NOK0020 | Start Date*: 2021-01-25 |
Sponsor Name:Nederlandse Obesitas Kliniek | ||
Full Title: Liraglutide for low-responders after bariatric surgery | ||
Medical condition: Morbid obesity | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2014-002970-36 | Sponsor Protocol Number: 54508 | Start Date*: 2016-06-06 |
Sponsor Name:Maastricht University Medical Center | ||
Full Title: Human intestinal ischemia and reperfusion | ||
Medical condition: The participants enrolled in this study will all undergo major upper abdominal surgery (i.e. mostly Pylorus Preserving Pancreatico Duodenectomy or whipple procedure) mostly for pancreatic cancer, p... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2021-002145-15 | Sponsor Protocol Number: NOK0023 | Start Date*: 2023-10-31 |
Sponsor Name:Nederlandse Obesitas Kliniek | ||
Full Title: Applying Mysimba in patients with weight regain after bariatric surgery | ||
Medical condition: Weight regain post bariatric surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2019-001915-22 | Sponsor Protocol Number: CKN-DASI-RYGB | Start Date*: 2019-09-05 | |||||||||||
Sponsor Name:Center for Clinical Metabolic Research at Herlev-Gentofte Hospital | |||||||||||||
Full Title: Dasiglucagon in the treatment of postprandial hypoglycaemia after Roux-en-Y gastric bypass | |||||||||||||
Medical condition: Postprandial hyperinsulinemic hypoglycaemia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
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