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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: 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.