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Abdominal Pain clinical trials

View clinical trials related to Abdominal Pain.

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NCT ID: NCT00413855 Completed - Clinical trials for Chronic or Recurrent Appendicitis

Laparoscopic Appendectomy for Chronic Right Lower Abdominal Pain

Start date: September 1994
Phase: Phase 3
Study type: Interventional

It is questionable whether elective appendectomy can effectively reduce pain in persistent or recurrent lower abdominal quadrant pain due to chronic appendicitis. A single centre randomised double-blind sham surgery controlled clinical trial studied the effects of elective laparoscopic appendectomy on postoperative pain perception in patients with persistent or recurrent lower abdominal quadrant pain on abdominal pain at 6 months postoperatively. Secondary outcome was the relation between clinical response and the appendix’ histopathology. The analysis was performed on an intention-to-treat basis. Pain scores were compared using a Fisher’s exact test.

NCT ID: NCT00327548 Completed - Clinical trials for Functional Abdominal Pain

Use of Guided Imagery for Functional Abdominal Pain in Children:

Start date: n/a
Phase: Phase 3
Study type: Interventional

The purpose of the study is to evaluate the effectiveness of relaxation, with or without guided imagery, for treating children with functional abdominal pain. The study will evaluate a child's ability to decrease the amount of pain with these techniques to allow continuation of normal daily activities at home and at school. The hypothesis is that these relaxation techniques will help decrease reports of abdominal pain and improve levels of activity.

NCT ID: NCT00311233 Completed - Abdominal Pain Clinical Trials

Recurrent Abdominal Pain in Childhood -Characteristics and Course

Start date: February 2006
Phase: N/A
Study type: Observational

Recurrent abdominal pain (RAP) is a common complaint in childhood. Identification of the processes that maintain illness is important. The purpose of this study is to get more knowledge about characteristics of children with recurrent abdominal pain and their parents, and about the course of their pain. These results may be important to identify children who need treatment.

NCT ID: NCT00310765 Terminated - Abdominal Pain Clinical Trials

Pregabalin for Abdominal Pain From Adhesions

Start date: March 2006
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate if pregabalin demonstrates significant reduction in abdominal pain from adhesions.

NCT ID: NCT00286286 Active, not recruiting - Obesity Clinical Trials

Intraperitoneal Aerosolized Delivery of a Local Anesthetic for Post Operative Pain Management. A Double Blind, Randomised Controlled Clinical Trial.

Start date: February 2006
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the effectiveness of aerosolized pain medication (.5% bupivicaine) delivered into the peritoneal cavity after laparoscopic gastric bypass surgery. This double blind study will include 50 patients. 25 will receive the aerosolized pain medication and 25 will receive a placebo (normal saline). All 50 patients will receive routine/typical methods of post-operative pain management. Post operative pain scores of the patients will be examined to determine the effect of aerosolization.

NCT ID: NCT00267618 Completed - Clinical trials for Pediatric Recurrent Headache & Abdominal Pain

Family Help Program: Pediatric Recurrent Headache and Abdominal Pain

Start date: June 2004
Phase: Phase 2
Study type: Interventional

The purpose of the Strongest Families (formerly Family Help Program)is to evaluate the effectiveness of the Strongest Families distance intervention compared to usual or standard care that is typically provided to children with mild to moderate Recurrent Headache/Abdominal Pain symptomology. This is a single-centre trial based at the IWK Health Centre. The primary outcome is change in diagnosis.

NCT ID: NCT00240123 Withdrawn - Abdominal Pain Clinical Trials

Effect of Benadryl Sedation During ERCP or EUS

Start date: July 2005
Phase: Phase 1
Study type: Interventional

The purpose of the study is to determine if adding Benadryl improves sedation for patients scheduled to undergo ERCP or EUS procedures.

NCT ID: NCT00225238 Completed - Nausea Clinical Trials

The Effects of Nexium on the Side Effects Associated With a Colonoscopy Prep

Start date: December 2003
Phase: Phase 4
Study type: Interventional

The purpose of this study is to ascertain if the use of Nexium for 7 days prior to taking a colon prep for a colonoscopy will decrease the side effects that are associated with the colon preparation

NCT ID: NCT00215280 Completed - Pruritus Clinical Trials

Epidemiology and Control of Mansonella Perstans Infection in Uganda

Start date: November 2005
Phase: N/A
Study type: Interventional

Mansonella perstans (M. perstans) infection is widespread in Uganda. Knowledge about the epidemiology of this infection, and of the morbidity it induces is poor, and no effective treatment is available. The study aims at providing data on diagnostic, epidemiological, morbidity and treatment aspects of M. perstans infections in Uganda.

NCT ID: NCT00209807 Recruiting - Pain Clinical Trials

Effect of Escitalopram vs. Reboxetine on Gastro-intestinal Sensitivity of Patients With Major Depressive Disorder

Start date: September 2005
Phase: Phase 4
Study type: Interventional

Patients with major depressive disorder (MDD) commonly have many gastrointestinal complaints. Gastrointestinal pain is classified into 2 categories: visceral and somatic pain. The main aim of this study is to compare somatic and visceral sensitivity between healthy people and pateints with MDD. These two sensitivities will be assessed by the 2 following tests: standardized rectal distension and Transdermal transcutaneous electric nerve stimulation. Thereafter, patients with MDD will be randomly allocated to escitalopram or reboxetine. After 6 weeks of treatment, somatic and visceral sensitivity will be reassessed.