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Gynecologic Diseases clinical trials

View clinical trials related to Gynecologic Diseases.

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NCT ID: NCT02811081 Completed - Clinical trials for Gynecologic Diseases

Effective Maneuver for Post-laparoscopic Shoulder Pain

Start date: June 26, 2016
Phase: N/A
Study type: Interventional

The aim of this clinical trial is to estimate the efficacy and safety of combined intervention with the intra-peritoneal normal saline instillation and pulmonary recruitment maneuver for reducing post-laparoscopic shoulder pain.

NCT ID: NCT02729272 Completed - Clinical trials for Gynecologic Diseases

Ultrasonic Versus Monopolar Energy-based Surgical Device in Colpotomy

ULMOST
Start date: April 2016
Phase: N/A
Study type: Interventional

The aim of this randomized trial was to compare the degree of surgical smoke obstructing vision and thermal damage caused by two different ESDs (ultrasonic versus monopolar ESD) in colpotomy during total laparoscopic hysterectomy.

NCT ID: NCT02654808 Completed - Clinical trials for Gynecologic Diseases

AirSeal®Insufflation Trocar/CO2 Absorption Study

Start date: May 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to compare carbon dioxide (CO2) absorption during gynecologic laparoscopy using the AirSeal® valveless trocar system versus standard insufflation trocars at intra-abdominal pressures of 10 and 15 mmHg. The investigators hypothesize that with the AirSeal® valveless trocar system, gynecologic laparoscopy can be performed at a lower intra-abdominal pressure with a possible resultant decrease in CO2 absorption, while maintaining adequate visualization of the operative field for safe completion of surgery.

NCT ID: NCT02596425 Completed - Clinical trials for Gynecologic Diseases

Pulmonary Recruitment Maneuver for Postlaparoscopic Shoulder Pain

Start date: November 2015
Phase: Phase 3
Study type: Interventional

The aim of this clinical trial is to evaluate the efficacy and safety of different recruitment maneuvers for reducing postlaparoscopic shoulder pain.

NCT ID: NCT02567838 Completed - Clinical trials for Gynecologic Diseases

Lidocaine Gel During Transrectal Sonography

Start date: October 2015
Phase: Phase 3
Study type: Interventional

The aim of this clinical trial is to evaluate the use of topical lidocaine gel in reducing pain associated with transrectal ultrasonography (TRS) in gynecologic field.

NCT ID: NCT02357251 Completed - Laparotomy Clinical Trials

Enhanced Recovery After Surgery: A RCT of Perioperative Management of Gynecologic Patients

Start date: December 12, 2014
Phase: N/A
Study type: Interventional

This is a single-blinded randomized control trial comparing the current perioperative care of the investigators gynecologic oncology patients with a standardized perioperative "enhanced recovery" pathway. Adult patients undergoing laparotomy by one of the gynecologic oncology surgeons will be eligible to participate. The primary outcome will be length of hospitalization including any days of readmission in the 30 days post-operatively. Secondary outcomes will include 30-day readmission rate, complications, quality of recovery, and pain control.

NCT ID: NCT00734812 Withdrawn - Clinical trials for Gynecologic Diseases

Laparoscopic Supracervical Hysterectomy Versus Total Laparoscopic Hysterectomy

Start date: May 2008
Phase: Phase 3
Study type: Interventional

The purpose of this research study is to evaluate whether there is any difference in recovery time and return to normal activities following a laparoscopic supracervical hysterectomy (LSH) compared with total laparoscopic hysterectomy (TLH). Both types of hysterectomies are commonly performed at our institution. Patients will be assigned by chance (like a coin toss) to have either a LSH or a TLH. Preoperatively, participants will complete a quality of life questionnaire (SF-36), a sexual function questionnaire (FSFI)and a 3 question questionnaire about urinary function (3IQ). Following surgery participants will be asked to keep a diary of pain symptoms and use of narcotics. The diary will be filled out daily until patients have resumed normal activities from prior to the surgery. The SF-36 will be completed again 6 weeks following the original surgery. 6 months following surgery participants will receive a copy of the SF-36 and the FSFI in the mail. They will also be asked questions about urinary symptoms and persistent vaginal bleeding.

NCT ID: NCT00526331 Completed - Prostate Cancer Clinical Trials

Evaluation of Arterial Pressure Based Cardiac Output for Goal-Directed Perioperative Therapy

Start date: August 2007
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether the early identification and more precise intervention of operating room (OR) patient fluid administration optimization using arterial pressure-based cardiac output (APCO) yields comparable patient outcome as fluid administration optimization using a global standard care method.

NCT ID: NCT00456924 Completed - Contraception Clinical Trials

Low Dose Continuous Administration of the Progesterone Receptor Modulator VA2914

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

The purpose of the present study is to evaluate continuous administration of low doses of VA2914 for potential contraceptive activity and effects on the menstrual cycle and steroid hormone parameters.