EVeRLAST 2-Year Follow-Up
NCT05542836 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 63
Last updated 2024-12-06
Summary
This is a 2-year follow-up study from EVeRLAST which objective was to determine whether expedited resumption of postoperative activity levels is non-inferior to standard activity restrictions with respect to short-term anatomic prolapse outcomes. The preliminary data from the original study suggest expedited instructions are non-inferior. We hypothesize this effect continues at the 2-year postoperative mark and patients continue to have non-inferior outcomes after prolapse surgery when compared to standard postoperative activity restrictions.
Participants from the original EVeRLAST will be approached to assess their interest in participating in the 2-year follow up study. We will be collecting objective and subjective data.
Conditions
- Pelvic Organ Prolapse
Interventions
- BEHAVIORAL
-
Expedited postoperative activity instructions
Ad lib postoperative activity and return to work recommendations
- BEHAVIORAL
-
Standard postoperative activity restructions
Standard conservative postoperative activity and return to work recommendations
Sponsors & Collaborators
- lead OTHER
Eligibility
- Sex
- FEMALE
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2022-09-30
- Primary Completion
- 2023-09-27
- Completion
- 2023-09-27
Countries
- United States
Study Locations
More Related Trials
-
Study of the Elevate Apical and Posterior Prolapse Repair System Compared to Native Tissue Repair for Pelvic Organ Prolapse
NCT02123992 ·Status: TERMINATED ·Phase: PHASE4
-
Study of the Elevate Anterior and Apical Prolapse Repair System Compared to Native Tissue Repair for Pelvic Organ Prolapse
NCT02121977 ·Status: TERMINATED ·Phase: PHASE4
-
Physical Therapy on Pelvic Organ Prolapse
NCT03244397 ·Status: COMPLETED ·Phase: NA
-
Restricted Convalescence: Outcomes Following Urogynecologic Procedures
NCT02138487 ·Status: COMPLETED ·Phase: NA
-
Evaluation of the Avaulta Procedure for the Correction of Pelvic Organ Prolapse - Results at 1 Year
NCT00774215 ·Status: COMPLETED
-
Quality of Life After Conservative and Surgical Treatment of Pelvic Organ Prolapse
NCT04110821 ·Status: RECRUITING
-
Exair® Versus Native Tissue Repair for Prolapse
NCT02162628 ·Status: TERMINATED
-
A Feasibility Study on the Value of Pelvic Floor Training After Pelvic Organ Prolapse Surgery
NCT04539782 ·Status: UNKNOWN ·Phase: NA
-
Platelet Rich Plasma as an Adjunct Therapy at the Time of Transvaginal Native Tissue Prolapse Surgery
NCT05731284 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
Effect of a Risk Calculator on Patient Satisfaction With the Decision for Midurethral Sling During Prolapse Surgery
NCT02111642 ·Status: COMPLETED ·Phase: NA
-
Early Versus Late Voiding Trials After Prolapse Repair
NCT02739256 ·Status: TERMINATED ·Phase: NA
-
Pelvic Floor Exercise Before Surgery in Women With Pelvic Organ Prolapse
NCT03064750 ·Status: COMPLETED ·Phase: NA
-
Prediction of Postsurgical Symptomatic Outcomes With Preoperative Pessary Use
NCT02680145 ·Status: COMPLETED ·Phase: NA
-
Effect of Phenazopyridine on Prolapse Surgery Voiding Trials
NCT03065075 ·Status: COMPLETED ·Phase: PHASE3
-
Enhancing Patient Recall in Urogynecologic Surgery
NCT04010292 ·Status: UNKNOWN ·Phase: NA
-
Voiding Assessment Based on Minimum Spontaneous Void of 150 mL Compared to Retrograde Fill Method After Female Pelvic Floor Reconstructive Surgery
NCT03539107 ·Status: COMPLETED ·Phase: NA
-
Race, Ethnicity, Socioeconomic Status and Prolapse-rElated Decisional ConflicT
NCT04977141 ·Status: COMPLETED
-
PREgnancy-associated Pelvic Floor Health Knowledge And REDuction of Symptoms: The PREPARED Trial
NCT02947282 ·Status: COMPLETED ·Phase: NA
-
Postoperative Return to Sexual Activity
NCT05342090 ·Status: COMPLETED ·Phase: NA
-
Long-term Effectiveness of Abdominal Sacrocolpopexy for the Treatment of Pelvic Organ Prolapse
NCT00099372 ·Status: TERMINATED
-
Benefits of Peri-surgical Physical Therapy in the Management of III and IV Grades of Pelvic Organ Prolapse
NCT02846480 ·Status: COMPLETED ·Phase: NA
-
Efficacy of Retrograde Fill Vs Spontaneous Fill to Assess Voiding Function
NCT01091844 ·Status: COMPLETED ·Phase: NA
-
Treatment for Acute Postoperative Voiding Dysfunction
NCT01189136 ·Status: COMPLETED ·Phase: NA
-
Awareness of Gynaecologists About Role of Physical Therapy in Genital Prolapse
NCT06338852 ·Status: COMPLETED
-
Altis® 522 Trial - Treatment of Female Stress Urinary Incontinence
NCT02348112 ·Status: COMPLETED