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Abdominal Pain clinical trials

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NCT ID: NCT01339117 Completed - Clinical trials for Irritable Bowel Syndrome

Delivered Dietary Intervention for Children With Irritable Bowel Syndrome

Start date: January 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether a specific diet may help children with irritable bowel syndrome.

NCT ID: NCT01335945 Terminated - Pain Clinical Trials

Safety and Efficacy of Cryoablation for Abdominal Pain Associated With Pancreatic Cancer

Start date: August 2011
Phase: Phase 1
Study type: Interventional

CUC10-PAN09 will evaluate the safety and efficacy of cryoablation therapy on the relief of epigastric/abdominal pain associated with pancreatic cancer.

NCT ID: NCT01318369 Completed - Abdominal Pain Clinical Trials

Efficacy Study of Δ9-THC to Treat Chronic Abdominal Pain

Delta-pain
Start date: October 2011
Phase: Phase 2
Study type: Interventional

The main goal of this trial is to study the efficacy of Namisol® after a single dose of Δ9-THC in the treatment of pain resulting from chronic pancreatitis. Objective measures of pain processing, e.g. encephalography (EEG) and quantitative sensory testing (QST), are included to provide insight in underlying nociceptive processing.

NCT ID: NCT01316471 Completed - Chronic Pain Clinical Trials

Internet Intervention for Adolescents With Chronic Pain

Start date: May 2011
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the efficacy of a web-based (i.e., internet) behavioral program to reduce pain and improve functioning in children and adolescents with chronic pain. We hypothesize that children and adolescents in families that receive the web-based behavioral program will report reduced pain levels and improved daily functioning compared to children and their parents who receive online patient education.

NCT ID: NCT01295138 Not yet recruiting - Constipation Clinical Trials

Pilot Study of the Effect of Lactulose on Post Caesarean Section Constipation

Start date: February 2011
Phase: N/A
Study type: Interventional

Constipation following elective Caesarean sections (CS) is a common problem experienced by up to 50% of patients (1). The causes for this are multifactorial and include manipulation of the bowel during surgery, immobilisation and opiate based anaesthetic and analgesic techniques. To try to alleviate the problem of postoperative constipation, some anaesthetists prescribe postoperative lactulose in addition to postoperative analgesia, although no data exists that shows whether this has any beneficial effect on postoperative constipation. 1. Short term morbidity associated with Caesarean delivery. Hillan EM. Birth. 19 (4): 190-4).

NCT ID: NCT01269671 Withdrawn - Clinical trials for Irritable Bowel Syndrome

Efficacy of Combination Therapy vs Placebo for Pediatric Functional Abdominal Pain

FAP
Start date: January 2011
Phase: Phase 1
Study type: Interventional

IND application was submitted to FDA on November 17th.

NCT ID: NCT01255345 Recruiting - Clinical trials for Irritable Bowel Syndrome

Female Chronic Pelvic Pain

Female CPP
Start date: January 2011
Phase: N/A
Study type: Observational

The purpose of this study is to investigate the frequency and severity of chronic pelvic pain (CPP) in adult women living in Copenhagen Country and Zealand Country (total population 2,4 million), Denmark, in relation to selected factors, such as basic demographic and clinical factors, health related quality of life, physical activity and abnormal muscular findings in the pelvic area.

NCT ID: NCT01245023 Withdrawn - Clinical trials for Chronic Abdominal Pain

Adhesiolysis in Chronic Abdominal Pain

Start date: January 2014
Phase: N/A
Study type: Interventional

Laparoscopic adhesiolysis has been used in treatment of chronic abdominal pain. There has been only one previous controlled study, that stated laparoscopy alone had the same benefits than laparoscopic adhesiolysis. The aim of this study is to compare laparoscopic adhesiolysis with a placebo-procedure in chronic abdominal pain.

NCT ID: NCT01180556 Completed - Abdominal Pain Clinical Trials

Effect of Probiotics in Childhood Abdominal Pain

Start date: March 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the effect of probiotics in childhood recurrent abdominal pain. Patients will be randomly assigned to receive L. reuteri or placebo for 4 weeks with a follow up phase of additional 4 weeks.

NCT ID: NCT01159119 Terminated - Clinical trials for Chronic Pancreatitis

A Study of EUR-1066 in Subjects With Chronic Pancreatitis, Exocrine Pancreatic Insufficiency and Chronic Abdominal Pain

EUR-1066
Start date: August 2, 2010
Phase: Phase 1
Study type: Interventional

The purpose of this study is to evaluate two different treatments in subjects with chronic pancreatitis, exocrine pancreatic insufficiency and chronic abdominal pain.