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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00710502
Other study ID # 05626
Secondary ID
Status Completed
Phase Phase 1/Phase 2
First received July 2, 2008
Last updated December 14, 2009
Start date January 2009
Est. completion date December 2009

Study information

Verified date December 2009
Source North Texas Veterans Healthcare System
Contact n/a
Is FDA regulated No
Health authority Mexico: Ethics CommitteeUnited States: Federal Government
Study type Interventional

Clinical Trial Summary

Cholecystectomy is one of the most common general surgery procedures performed in the US today and is among top 10 procedures performed in U.S. hospitals annually, and biliary tract disease has been estimated to cost U.S. healthcare $5 billion/year. Laparoscopic cholecystectomy was introduced in the early 1990s and has become the standard surgical approach for the treatment of gallbladder disease. More than 500,000 cholecystectomy procedures are performed in the US every year. Laparoscopic cholecystectomy is now performed as an outpatient basis and is related to a very low complication rate. Laparoscopic cholecystectomy requires the use of multiple trocar incisions.

Natural Orifice Translumenal Endoscopic Surgery(NOTES) is a new type of surgical procedure currently being studied around the world. The idea of NOTES was developed several years ago in response to the concepts that patients would

1. realize the benefits of less invasive surgery by reducing the recovery time,

2. experience less physical discomfort associated with traditional procedures

3. have virtually no visible scarring following this type of surgery.

All of these advantages have spurred research and investigation forward, encouraging physicians and researchers to develop new equipment and techniques to use during NOTES procedures. Although the Natural Orifice Translumenal Endoscopic Surgery approach may hold tremendous potential, there are many issues that need to be addressed before this technique is introduced into clinical care.

The purpose of this study is to determine the safety, feasibility and short-term clinical outcomes (Phase I trial) of transvaginal NOTES cholecystectomy in female patients with symptomatic cholelithiasis and compare it to Laparoscopic Cholecystectomy (Phase II).

Hypothesis 1: Transvaginal NOTES cholecystectomy is safe and feasible in female patients with symptomatic cholelithiasis.

Hypothesis 2: The short term outcomes of Transvaginal NOTES cholecystectomy are comparable to Laparoscopic Cholecystectomy in female patients with symptomatic cholelithiasis.

Aim 1: Determine the safety of Transvaginal NOTES cholecystectomy. Aim 2: Determine the feasibility of Transvaginal NOTES cholecystectomy. Aim 3: Determine the short-term outcomes of Transvaginal NOTES cholecystectomy. Aim 4: Compare the short-term outcomes of Transvaginal NOTES cholecystectomy to Laparoscopic cholecystectomy.


Description:

Most recently, surgeons and endoscopists have focused on NOTES cholecystectomy. Access to the abdominal cavity to perform NOTES procedures has been obtained by transgastric, transvaginal, transvesical and transrectal approaches. The first successful NOTES procedure in humans was an appendectomy in India. Transvaginal NOTES cholecystectomy has been successfully performed and reported in a handful of cases in the US, Europe and South America. However, to date, there is lack of clinical trials that demonstrate the safety and feasibility of Transvaginal NOTES cholecystectomy in a larger group of patients.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date December 2009
Est. primary completion date December 2009
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

1. Adult (> 18 years old) female patients residents of Durango Mexico.

2. Patients who undergo elective surgery.

3. Patients with ultrasound documented symptomatic cholelithiasis, gallbladder polyps of biliary dyskinesia.

4. Patients capable of giving written informed consent for the study.

Exclusion Criteria:

1. Patients who have contraindications prohibiting general anesthesia.

2. Pregnancy.

3. Previous abdominal or gynecological procedures.

4. Uncontrollable medical or psychiatric conditions

5. Elderly > 65 y/o.

6. Body Mass Index > 35 mg/kg2.

7. Complicated or acute cholecystitis.

8. Elevation of liver function tests.

9. Acute abdomen.

10. Intra-abdominal abscess.

11. Coagulopathy.

12. Imperforated hymen.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
Transvaginal NOTES cholecystectomy
Under general anesthesia, patients will undergo Transvaginal NOTES cholecystectomy
Laparoscopic cholecystectomy
Under general anesthesia, patients will undergo standard Laparoscopic cholecystectomy

Locations

Country Name City State
Mexico Universidad Juarez del Estado de Durango, Mexico Durango

Sponsors (2)

Lead Sponsor Collaborator
Universidad Juárez del Estado de Durango Hospital Universitario La Paz

Country where clinical trial is conducted

Mexico, 

Outcome

Type Measure Description Time frame Safety issue
Primary Safety and Efficacy of Transvaginal NOTES cholecystectomy when compared to Laparoscopic cholecystectomy 12 months Yes
Secondary Short term outcomes of Transvaginal NOTES cholecystectomy when compared to Laparoscopic Cholecystectomy 12 months Yes
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