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Gynecologic Disease clinical trials

View clinical trials related to Gynecologic Disease.

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NCT ID: NCT03427840 Recruiting - Pain, Postoperative Clinical Trials

Superior Hypogastric Plexus Blockade in Laparoscopic Hysterectomy

Start date: March 18, 2018
Phase:
Study type: Observational

The primary indication for superior hypogastric plexus (SHP) block is visceral pelvic pain, most commonly from malignancy of the ovary, uterus, cervix, bladder, rectum or prostate. Per-cutaneous SHP blocks should be done under guidance of ultrasonography, fluoroscopy, magnetic resonance or computed tomography. During minimally invasive laparoscopic surgery, percutaneous technique can be done under the guidance of cameras.

NCT ID: NCT03395821 Recruiting - Gynecologic Disease Clinical Trials

Traditional Versus Virtual Reality for Surgical Skills for ObGyn Residents

SIMUTEC
Start date: December 22, 2017
Phase: N/A
Study type: Interventional

This study will verify if a comprehensive laparoscopic curriculum using virtual reality demonstrates skills transfer to the operating room, compared to the traditional teaching method.

NCT ID: NCT03347409 Completed - Surgery Clinical Trials

Validation of an ERAS Protocol in Gynecological Surgery

ERASGYNBS001
Start date: June 14, 2017
Phase: N/A
Study type: Interventional

Validation of ERAS interventional measures in elective gynecological surgery, for benign either malignant pathology.

NCT ID: NCT03327506 Recruiting - Gynecologic Disease Clinical Trials

Preoperative Hypnosis Versus Premedication in Gynecological Surgery

HYPNOGYN
Start date: November 27, 2018
Phase: Phase 4
Study type: Interventional

The aim of this study is to evaluate the efficacy of an hypnosis session, performed on the eve of a laparoscopic gynecological surgery, on the level of immediate preoperative anxiety measured by State-Trait Anxiety Index (STAI-Y) self-administered questionnaire compared to premedication by alprazolam®.

NCT ID: NCT03135353 Recruiting - Gynecologic Disease Clinical Trials

Saline Sonohystrography and Office Hysteroscopy in Evaluation of Cases of Abnormal Uterine Bleeding

Start date: April 20, 2017
Phase: N/A
Study type: Interventional

comparing the efficacy of the 3D saline infusion sonohysterography to the diagnostic office hysteroscopy in the diagnosis of the cause of abnormal uterine bleeding in females during their reproductive age

NCT ID: NCT03007654 Recruiting - Gynecologic Disease Clinical Trials

Evaluate Anti-adhesive Effect and Safety of a Mixed Solid of Poloxamer, Gelatin and Chitosan(Mediclore®)

antiadhesion
Start date: December 2016
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the efficacy and safety of Mediclore®, as an antiadhesive barrier, which is made of Poloxamer, Gelatin and Chitosan.

NCT ID: NCT02957500 Recruiting - Gynecologic Disease Clinical Trials

To Evaluate Anti-adhesive Effect and Safety of a Mixed Solid of Poloxamer, Gelatin and Chitosan(Mediclore®)

antiadhesion
Start date: November 22, 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the efficacy and safety of Mediclore®, as an antiadhesive barrier, which is made of Poloxamer, Gelatin and Chitosan.

NCT ID: NCT02476799 Completed - Gynecologic Disease Clinical Trials

Analgesic Effects of US Bilateral Rectus Sheath Block for Laparoscopic GY Surgery

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

Rectus sheath block (RSB) is a kind of anterior abdominal wall block. It has postoperative analgesic effect for abdominal surgery with midline incision. Laparoscopic gynecologic surgery is accompanied by significant postoperative pain and usually IV-PCA is used to manage the pain.The purpose of this study is to investigate the analgesic effect of ultrasound-guided RSB to multi-port laparoscopic gynecologic surgery which has incision site at umbilical area. Patients will randomly assigned to two groups, RSB group and Control group. Each patients will assessed for time to first rescue analgesia, verbal numerical rating pain scores, number of rescue analgesic demands, and postoperatively opioids use by IV-PCA by a blinded investigator at 0, 1, 6, 12, 24 and 48 hours postoperatively.

NCT ID: NCT02450084 Completed - Gynecologic Disease Clinical Trials

Ultrasound-guided Bilateral Rectus Sheath Block for Robotic Single-port Gynecologic Surgery

Start date: May 2015
Phase: N/A
Study type: Interventional

Rectus sheath block (RSB) is a kind of anterior abdominal wall block. It has postoperative analgesic effect for abdominal surgery with midline incision. Robotic gynecologic surgery is accompanied by significant postoperative pain and usually IV-PCA is used to manage the pain.The purpose of this study is to investigate the analgesic effect of ultrasound-guided RSB to single-port robotic gynecologic surgery which has incision site at umbilical area. Patients will randomly assigned to two groups, RSB group and Control group. Each patients will assessed for time to first rescue analgesia, verbal numerical rating pain scores, number of rescue analgesic demands, and postoperatively opioids use by IV-PCA by a blinded investigator at 0, 1, 6, 12, 24 and 48 hours postoperatively.

NCT ID: NCT02097628 Not yet recruiting - Gynecologic Disease Clinical Trials

Comparison of Two Ventilation Modes With Laryngeal Mask Airway Guardian

wang002
Start date: April 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to compare volume- and pressure- controlled ventilation with laryngeal mask airway Guardian in obese patients undergoing laparoscopic gynecologic surgery in terms of ventilatory efficacy, airway leak pressure (airway protection), ease-of-use and complications.