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Relapse prophylaxis and early recognition of pelvic organ prolapse in primary medical care organizations

Optimization of the surgical treatment of genital prolapse

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN23741622
Enrollment
60
Registered
2023-01-30
Start date
2021-08-01
Completion date
Unknown
Last updated
2023-03-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Prevention of recurrence of genital prolapse after surgical treatment Nervous System Diseases

Interventions

The study aims to prevent the recurrence of genital prolapse after surgical treatment (anterior and posterior colpotomy, colporrhaphy with perineal levatorplasty) using a combination of a 6-month cour

Sponsors

Kazakhstan Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Anterior and posterior vaginal wall prolapse stage II, according to the Pelvic Organ Prolapse Quantification System (POP-Q) classification and stress-induced urinary incontinence stage III, which was determined by the classification of D.V. Kahn 2. Aged 45 years old and under 3. History of two or more labours 4. No consent for conservative treatment 5. No consent for use of vaginal synthetic prostheses, including urethral sling 6. No history of conservative treatment of prolapse, including pelvic floor muscles training 7. No history of metabolic diseases (diabetes mellitus, obesity, metabolic syndrome, thyroid gland disorders, calcium phosphate metabolism disorders)

Exclusion criteria

Exclusion criteria: 1. Urgent or combined urinary incontinence 2. Contraindications to surgical treatment and anaesthesia (general and regional anaesthesia: spinal, epidural anaesthesia) 3. Acute or chronic inflammatory diseases, acute phase of infectious diseases, malignant tumours, anaemia, benign ovarian and/or uterine tumours, pregnancy, haemorrhoids stage 3 and 4, decompensated chronic diseases, thrombosis and multiple drug allergies

Design outcomes

Primary

MeasureTime frame
Presence of anatomical prolapse measured during gynecological examination using POP-Q international scale for the estimation of prolapse stage prior to treatment and 8 months after surgical operation

Secondary

MeasureTime frame
Helath-related quality of life measured using the Prolapse Quality of Life Questionnaire (P-QoL) in Russian and Kazakh languages prior to treatment and 8 months after treatment.

Countries

Kazakhstan

Contacts

Public ContactBarmanasheva;Imasheva Zauresh;Bayan Imashkyzy

;

Ingling-freia@mail.ru;imasheva_bayan@inbox.ru+7 701 402 9691;None provided

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026