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Gynecological Disease clinical trials

View clinical trials related to Gynecological Disease.

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NCT ID: NCT05687227 Completed - Clinical trials for Gynecological Disease

Online Education and Counseling Regarding Gynecological Examination

Start date: June 4, 2021
Phase: N/A
Study type: Interventional

This research was carried out to determine the effect of online education and counseling on women's attitudes and anxiety levels regarding gynecological examination. The research is a pre-test-post-test, randomized controlled experimental study.

NCT ID: NCT05401058 Recruiting - Urologic Diseases Clinical Trials

Low-dose Droperidol for Prevention of Postoperative Delirium in Elderly Patients After Non-cardiac Surgery

Start date: November 21, 2022
Phase: N/A
Study type: Interventional

The aim of this multicenter, prospective, randomized, double-blind and large sample study is to explore the preventive effect of low-dose droperidol on POD in elderly patients after non-cardiac surgery, providing new approach for reducing the incidence of POD and improving the prognosis and quality of life.

NCT ID: NCT05276882 Recruiting - Clinical trials for Gynecological Disease

Improved Rehabilitation After Surgery and Hypnosis: Benefits Potentiated by a Preoperative Consultation

RACHYP
Start date: December 8, 2022
Phase: N/A
Study type: Interventional

Today, patient management in the context of scheduled surgery must meet new requirements. The understanding of surgical aggression, the evolution of anesthesia and surgery techniques have allowed the birth of the protocol of Improved Rehabilitation After Surgery. The objective is a pain-free surgery, with a minimum of risks, with a global management of the patient and an active participation. In 2019, the Nice University Hospital developed this program. Other non-medicinal techniques could promote the evolution of this program such as integrative medicine with, in this study case, hypnosis. Since 2002, thanks to its widely recognized effectiveness in the treatment of pain and in helping with care, its use has developed. A hypnosis session, proposed in the preoperative period, would considerably reduce the patient's anxiety, postoperative pain, a better and faster recovery with an easier healing: objectives of the Improved Rehabilitation After Surgery program. The patient's satisfaction would also be improved thanks to his active participation, in a greater comfort, which the investigators want to demonstrate by our work.

NCT ID: NCT01639599 Completed - Clinical trials for Gynecological Disease

Optimal Haloperidol Dose for Postoperative Nausea and Vomiting Prevention in High-risk Patients

Start date: March 2012
Phase: N/A
Study type: Interventional

Low-dose haloperidol is known to be effective for the treatment of postoperative nausea and vomiting (PONV). However, precise dose-response studies have not been completed, especially in patients at high risk for PONV who require combination therapy. This study sought to identify the optimal dose of haloperidol that could be combined with dexamethasone without adverse effects in high-risk PONV patients receiving intravenous patient-controlled anesthesia (IV PCA) after gynecological laparoscopic surgery.

NCT ID: NCT01437462 Completed - Healthy Adults Clinical Trials

Sevoflurane, Propofol, Postoperative Pain

Start date: October 2008
Phase: Phase 4
Study type: Interventional

The impact of anaesthetic method (intravenous vs. inhalational) has been proposed, but not proven in a large-scale study. The researchers aim to provide an investigation that has sufficient power to clarify the potential effect of anaesthetic method on postoperative need of opioids. Sevoflurane and propofol will be compared.