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Vaginal Hysterectomy clinical trials

View clinical trials related to Vaginal Hysterectomy.

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NCT ID: NCT01079754 Recruiting - Pain Clinical Trials

0.05 Versus 0.1 mg Spinal Morphine for Reducing Morphine Requirement After Vaginal Hysterectomy

Start date: March 2010
Phase: Phase 4
Study type: Interventional

This study aims to compare the efficacy of 0.05 mg and 0.1 mg spinal morphine in reducing postoperative morphine requirement in patients undergoing vaginal hysterectomy with/without anterior and posterior vaginoplasty.

NCT ID: NCT00456170 Not yet recruiting - Clinical trials for Vaginal Hysterectomy

Are Sutures Required for Vaginal Hysterectomy: A Randomized Controlled Trial

HAVE
Start date: April 2007
Phase: Phase 1
Study type: Interventional

The hypotheses of this study is that the use of the instrument “Harmonic Scalpel” (ultrasonic shears) for vaginal hysterectomy instead of traditional sutures confers advantage over the use of traditional clamps and sutures. The proposed benefits and outcome measures are reduced blood loss, reduced operating time, reduced post-operative pain and earlier discharge from hospital. Other outcome measure will include complications and cost.

NCT ID: NCT00222326 Completed - Clinical trials for Vaginal Hysterectomy

The Effect of Physiotherapy Treatment Following Gynaecological Surgery

Start date: July 2002
Phase: N/A
Study type: Interventional

Optimal pelvic floor muscle function is known to assist bladder and bowel function and control, pelvic organ support, as well as other areas of health. It is also known that problems in some of tehse areas can be a consequence of pelvic surgery. By addressing the requirements for good bladder and bowel function/control, and organ support in the early post-surgery phase when tissue repair and scar formation are critical, it is proposed that there will be a rduction in the longterm prevalence of bladder problems, bowel difficulties and weakened pelvic floor and abdominal muscles in post-surgery patients. This study is a randomised controlled trial to compare patients undergoing a physiotherapy-supervised pelvic floor muscle training and behavioural therapy program with a control group. It is hypothesised that at the 12 month post-operative follow-up assessment, the treatment group will demonstrate better outcomes in bladder and bowel function and control, as well as stronger pelvic floor muscle contractile strength than the control group.