Clinical Trials Logo

Appendicitis clinical trials

View clinical trials related to Appendicitis.

Filter by:

NCT ID: NCT00565682 Completed - Clinical trials for Laparoscopic Surgery for Cholecystitis

Pain Post Abdominal Laparoscopy Prevention With Arcoxia

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

To test the analgesic efficacy of etoricoxib used before a surgical procedure compared to the already known effect when administered after such a procedure. Patient will be receiving either etoricoxib or the respective placebo one hour before surgery, then two hours after those receiving the active will receive placebo and those that received placebo will be given etoricoxib. Pain score measurements will be performed sequentially. Rescue medication will be available all the time.

NCT ID: NCT00554008 Completed - Appendicitis Clinical Trials

Comparative Study of Laparoscopic Versus Open Appendectomy in Children

Start date: December 2007
Phase: N/A
Study type: Interventional

The study intends to compare the results of two surgical methods to remove the appendix in children with appendicitis. Specifically, up to 500 children over 3 years will be placed in two groups where the only difference in treatment is open or laparoscopic (scope) operation. Each group will be tracked for their baseline characteristics, events during operation and recovery, pain medication requirements, duration of hospital stay, and patient/family satisfaction. The investigators hypothesize that their will be no difference in the parameters measured between the techniques of appendix removal.

NCT ID: NCT00552162 Completed - Appendicitis Clinical Trials

NOTES Transvaginal Cholecystectomy and Appendectomy

Start date: June 2008
Phase: N/A
Study type: Interventional

Natural Orifice Translumenal Endoscopic Surgery (NOTES) is considered by many leading expert surgeons to be the next step in MIS (Minimally Invasive Surgery). This is a rapidly evolving area of preclinical research and several groups worldwide are developing this surgical approach together with industry support. In this new surgical technique, abdominal operations are performed using the oropharynx, rectum, or vagina as the ports of entry to the peritoneal cavity instead of incisions on the abdominal wall. NOTES offers all the advantages of minimally invasive surgery (MIS) and also completely eliminates trauma to the abdominal wall and the numerous complications of abdominal wall incisions. A NOTES procedure eliminates any visible scar and could also potentially reduce post operative pain due to the elimination of abdominal wall trauma. In this trial we intend to operate healthy women who need to undergo cholecystectomy or appendectomy. The operations will be performed through the vagina as the access port to the peritoneum and it will be monitored with laparoscopic vision for safety reasons.

NCT ID: NCT00530998 Completed - Appendicitis Clinical Trials

Minimally Invasive Surgery: Using Natural Orfices

NOTES
Start date: September 2007
Phase:
Study type: Observational

This is an observational study of pain and outcomes from females undergoing transvaginal NOTES removal of their appendix or gallbladder. Female subjects who elect to have a transvaginal NOTES removal of their appendix or gallbladder and agree to be in this study (through signature on the informed consent form) will be followed per standard of care, with additional follow-up for data collection including the following: - Subjects will complete a 7 day pain/temperature log after surgery - Subjects will complete a standardized sexual function questionnaire (Female Sexual Function Index) prior to surgery and 6 months after surgery - Subjects will receive a phone call at 6 months and at 1 year after surgery to capture data related to safety, adverse events, hospitalizations and patient satisfaction Additional data related to pain and outcomes will be collected at baseline/screening and at follow-up as necessary.

NCT ID: NCT00528138 Completed - Clinical trials for Perforated Appendicitis

Hyperbilirubinemia in Acute Appendicitis as a Predictor of Perforation

Start date: October 2007
Phase: N/A
Study type: Observational

It has recently been published that hyperbilirubinemia is a reliable marker for the preoperative diagnosis of perforated acute appendicitis. The investigators believe, based on their own previous publications, that C-reactive protein (CRP) with or without a white blood cell count and some other clinical parameters, are more specific markers for the preoperative diagnosis of perforated acute appendicitis. The purpose of this study is to prospectively compare the specificity and sensitivity of hyperbilirubinemia CRP, white blood cell count and other clinical parameters for the preoperative diagnosis of acute appendicitis.

NCT ID: NCT00477061 Completed - Appendicitis Clinical Trials

Morphine Analgesia in Patients With Acute Appendicitis

Start date: January 2004
Phase: Phase 4
Study type: Interventional

The purpose of the study is to evaluate morphine effect on pain reduction and diagnostic accuracy in patients admitted to emergency ward with the diagnosis of acute appendicitis.

NCT ID: NCT00469430 Completed - Appendicitis Clinical Trials

Study of Conservative Versus Surgical Treatment of Appendicitis

Start date: May 2006
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine if antibiotic treatment of appendicitis is an option compared to surgery. The investigators' hypothesis is that a majority of patients with appendicitis can heal without surgery and that there are several advantages with antibiotic treatment related to time to recover, complications and economical aspects.

NCT ID: NCT00462020 Completed - Clinical trials for Perforated Appendicitis

Intravenous Versus Intravenous/Oral Antibiotics for Perforated Appendicitis

Start date: March 2007
Phase: N/A
Study type: Interventional

The objective of this study is to scientifically evaluate two different management strategies for perforated appendicitis. The hypothesis is that early discharge with oral antibiotic therapy may result in a dramatic decrease in medical care expenses for the patient. The primary outcome variable between the two strategies is abscess rate.

NCT ID: NCT00435032 Completed - Clinical trials for Ruptured Appendicitis

Early Versus Interval Appendectomy for Ruptured Appendicitis in Children

RAPTOR
Start date: October 2006
Phase: Phase 3
Study type: Interventional

The purpose of this randomized trial is to compare two commonly utilized surgical treatments for children with ruptured appendicitis: early appendectomy, versus interval appendectomy. The primary outcome measure is time away from normal activities.

NCT ID: NCT00414375 Completed - Appendiceal Abscess Clinical Trials

Early Versus Delayed Operation for Perforated Appendicitis

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

The objective of this study is to scientifically evaluate two different operative strategies for perforated appendicitis with abscess. The hypothesis is that the increased difficulty of early operation is balanced by the immense patient investment with delayed operation.