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Prolapse; Female clinical trials

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NCT ID: NCT05978414 Recruiting - Clinical trials for Endometriosis-related Pain

Functional Links Between the Temporomandibular Joint and the Pelvis in Gynecology

TMJ and Pelvis
Start date: November 14, 2023
Phase: N/A
Study type: Interventional

1 Recruitment. 2. Collection of written consents for the study. 3. Random assignment to groups with and without intervention. 4. Completion of questionnaires by study participants, postural pattern assessment, temporomandibular joint assessment, and platform assessment. 5. Performance of visceral therapy in the group with intervention, in the group without intervention placebo. Duration 5 weeks, treatment 1x per week at the same time of day and given day e.g. Mondays only. 6. Reassessment as in step 4. 7. Data collection, statistical analyses. 8. Interpretation of results for female participants. 9. Preparation of results for scientific publications.

NCT ID: NCT05836844 Recruiting - Prolapse; Female Clinical Trials

Pragmatic Evaluation of Performance and Safety of the Anchorsure® Transvaginal Device for Surgical Treatment of Apical Prolapse in Women

APAS
Start date: May 11, 2023
Phase:
Study type: Observational

Pelvic Organ Prolapse affects 50% of parous women, and apical prolapse is one of the most common types of prolapse. Treatment for apical prolapse ranges from observation, non-surgical treatment or surgical repair. An anchoring device can reduce dissection and operative time and is meant to provide strong fixation whilst minimizing potential postoperative pain by avoiding neurovascular injuries. These potential advantages must be evaluated in terms of performance and safety. This cohort study will be on patients undergoing sacrospinous fixation with the Anchorsure® system with a follow-up of 36 months.

NCT ID: NCT05760794 Recruiting - Prolapse; Female Clinical Trials

Barbed-suture Efficiency Study for Sacrocolpopexy

BEST
Start date: June 21, 2023
Phase: N/A
Study type: Interventional

Minimally invasive sacrocolpopexy (SCP) performed laparoscopically or with robotic assistance is associated with improved patient-centered outcomes such as faster recovery times, less pain, less bleeding, and shorter hospital stay, however at the expense of longer operating times. One of the time consuming parts of the procedure is vaginal mesh attachment.

NCT ID: NCT05750615 Recruiting - Prolapse; Female Clinical Trials

What Affects Willingness to Self-manage a Pessary?

Start date: August 25, 2022
Phase:
Study type: Observational

Pessary self-management is defined as the patient's ability to remove and reinsert their pessary themselves at home. Previous research has suggested that some women may prefer being able to remove and reinsert their pessary as they wish rather than wait for clinic appointments. At the moment, not enough is known about pessary self-management, particularly what makes someone more or less likely to try pessary self-management. The investigators would like to understand this better to try to help women overcome barriers they might face. This study aims to collect data via both questionnaires and interviews to explore willingness to self-manage a pessary. Using findings from the questionnaires and interviews, a group of women who use pessaries and healthcare professionals who provide pessary care will work together to develop a better way to support women to feel able and willing to manage their pessary in future.

NCT ID: NCT05633901 Recruiting - Prolapse; Female Clinical Trials

Impact of Preop Video on Patient Anxiety

Start date: December 7, 2022
Phase: N/A
Study type: Interventional

To determine whether a pre-operative educational video has an impact on the anxiety of patients undergoing vaginal prolapse surgery

NCT ID: NCT04880239 Recruiting - Prolapse; Female Clinical Trials

REDUCE Trial- Reducing Prolapse Recurrence

Start date: November 23, 2021
Phase: N/A
Study type: Interventional

This study will examine whether surgeons should add a prophylactic posterior colpoperineorrhaphy to a mesh-augmented apical prolapse repair.

NCT ID: NCT04440475 Recruiting - Pain, Postoperative Clinical Trials

Tap Block vs Conventional Pain Medication for Patients Undergoing Robotic Sacrocolpopexy

SACROTAP
Start date: June 28, 2020
Phase: N/A
Study type: Interventional

The purpose of this study is to assess whether the transversus abdominis plane block (Tap block) is different than the oral postoperative pain medications in controlling pain after robotic sacrocolpopexy.