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Hysterectomy clinical trials

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NCT ID: NCT06340776 Completed - Vomiting Clinical Trials

The Effects of Acupressure on Pain, and Gastrointestinal Functions in Women With Hysterectomy

Start date: August 15, 2021
Phase: N/A
Study type: Interventional

Aim This randomized controlled trial was conducted to evaluate the effect of acupressure application on gastrointestinal functions and pain after abdominal hysterectomy. Materials and methods After undergoing hysterectomy, 39 women were randomised into acupressure (n=19), and control groups (n=20). Women in the acupressure group received acupressure on the mide meridian (ST36), the heart meridian (HT7), large intestine meridian (LI4), intersection of the spleen, liver and kidney meridians 6(SP6) and pericardium meridian (PC6) acupoints 30 min after admission to the clinic, for a period of 15 min, whereas those in the sham group received acupressure on locations 1-1.5 cm away from these points. The control group received standard treatment. The patient information form, Visual analog scale, the Rhodes Index of Nausea, Vomiting and Retching, and daily follow-up form were used for data collection.

NCT ID: NCT05659303 Completed - Hysterectomy Clinical Trials

Evaluation of an Outpatient Protocol in Patients Operated for Laparoscopic Hysterectomy

HYSTECOE
Start date: October 15, 2022
Phase:
Study type: Observational

Removal of the uterus, or hysterectomy, is a surgical operation that involves partial or total removal of the uterus. It can be done by vaginally, laparoscopically or laparotomically. Since the first hysterectomy performed by laparoscopy in 1989, this approach has gained popularity to varying degrees depending on the countries. This technique allows a major surgical procedure to be performed by incisions of only a few millimeters, thus reducing parietal pain and visceral in addition to a cosmetic benefit. Since 2013, more than 200 laparoscopic hysterectomies have been scheduled on an outpatient basis at the Clinique des Cèdres (France). The analysis of this retrospective series of approximately 200 patients would provide elements related to the practice of laparoscopic hysterectomy in ambulatory in France.

NCT ID: NCT05654363 Completed - Pain, Postoperative Clinical Trials

Observational Retrospective Study on Spinal Analgesia in Laparoscopic and Laparotomic Hysterectomy

SPIN_GYN
Start date: March 13, 2023
Phase:
Study type: Observational

Perioperative multimodal analgesia, defined by the use of various analgesic medications targeting different drug receptors, provides adequate pain relief with minimal or no opiate consumption. Therefore, it represents one of the cornerstone of Enhanced Recovery After Surgery (ERAS) protocols, as the reduction in opioid use and the associated side effects may eventually reduce length of hospital stay, increase patient satisfaction and minimise the risk of long-term opioid use. Regional and neuraxial anesthesia techniques are key interventions to provide successful analgesia in the context of a multimodal strategy. Intrathecal morphine, for its effectiveness and potential of reducing the need of intravenous postoperative opioids, seems an attractive option in the case of hysterectomy, one of the most common major surgical procedures performed in women, associated with severe postoperative pain even when performed laparoscopically. The aim of our observational retrospective study is therefore to compare the analgesic efficacy and the safety of morphine administered by intrathecal route versus intravenous route during the first 48 hours after performance of laparoscopic/laparotomic hysterectomy.

NCT ID: NCT05610384 Completed - Postoperative Pain Clinical Trials

Ibuprofen Versus Ketorolac for Perioperative Pain Control After Open Hysterectomy

Start date: November 20, 2022
Phase: N/A
Study type: Interventional

The aim of this study is to compare the analgesic effect of intravenous ibuprofen to ketorolac for pain control after open hysterectomy

NCT ID: NCT05436691 Completed - Anxiety Clinical Trials

The Effect of Information and Coping With Anxiety Training Given to Women Before Hysterectomy on Their Level of Anxiety

Start date: July 15, 2018
Phase: N/A
Study type: Interventional

Purpose: In this study, it was aimed to determine the effect of information and coping with anxiety training given to women before they undergo hysterectomy on their anxiety levels. Design and Methods: The parallel group post-test randomized controlled experimental design was used in the study. The study sample comprised 59 women.

NCT ID: NCT05406960 Completed - Hysterectomy Clinical Trials

Therapeutic Effect of Herbal Infusion on Menometrorrhagia

HERBALTREAT
Start date: May 10, 2019
Phase: N/A
Study type: Interventional

This is an interventional, non-randomized, controlled, pilot study that explores a new approach to treat, Abnormal uterine bleeding-menometrorrhagia in women, being candidates for hysterectomy, based on tea infusion consumption of a mixture of two plants.

NCT ID: NCT05270447 Completed - Pain Clinical Trials

Short-Term Effects of Connective Tissue Massage After Hysterectomy

Start date: October 12, 2020
Phase: N/A
Study type: Interventional

The aim of this study to investigate the effects of connective tissue massage (CTM) on pain, intestinal peristaltism and functionality after total laparoscopic (TLH) or abdominal hysterectomy (TAH). Patients who underwent TLH randomly group as TLH-CTM (n=15) and TLH control (n=16), and TAH randomly group as TAH-CTM (n=14) and TAH control (n=15). The postoperative daily monitoring sheet, Visual Analogue Scale (VAS), time of intestinal peristaltism employees to collect research data.

NCT ID: NCT05190939 Completed - Hysterectomy Clinical Trials

The Use of Dye-less Cystoscopy in Assessing Urinary Tract Integrity During Hysterectomy

Start date: July 1, 2018
Phase: N/A
Study type: Interventional

An investigation comparing the reliability of dye-aided versus dye-less evaluation of urinary tract integrity during intra-operative cystoscopy among patients undergoing hysterectomy.

NCT ID: NCT05080114 Completed - Surgery Clinical Trials

Vaginal Cuff Closure by Modification of the Bakay Technique in Total Laparoscopic Hysterectomy

Start date: November 1, 2018
Phase: N/A
Study type: Interventional

Modified Bakay technique offers a novel colpotomy and cuff closure technique for total laparoscopic hysterectomy (TLH), and consists of placing a single continuous running purse-string suture facilitating the cuff closure before colpotomy. The modified Bakay technique adds a standard apical compartment support and has the potential to facilitate the primary healing of the vaginal cuff. This study aimed to compare the surgical and clinical outcomes of the Modified Bakay technique to conventional standard technique in patients undergoing TLH.

NCT ID: NCT05063864 Completed - Hysterectomy Clinical Trials

Post-Hysterectomy Nursing Support Program

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

Objective: This study was conducted to evaluate the effectiveness of the nursing support program developed for women undergoing hysterectomy. Background: Hysterectomy is an important surgical intervention that affects women physically, sexually and psychosocially. Method: The study is a single blind, randomized controlled study conducted at the Department of Obstetrics and Gynecology in a university hospital between November 2017 and November 2018. 60 women who had hysterectomy were divided into experimental and control groups and It was evaluated on the 1-2 day, 6-7 day and 2nd month. In the study, the nursing support program was applied only to women in the experimental group.