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The effect of perineuropathy and posterior anterior repair (APR) in postoperative patients

The effect of perineuropathy and posterior anterior repair (APR) on body image, sexual function and quality of life in postoperative women

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20160521027998N9
Enrollment
119
Registered
2021-04-15
Start date
2021-02-19
Completion date
Unknown
Last updated
2021-04-26

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

Conditions

Condition 1: Rectocell. Condition 2: Cystocell. Condition 3: uterine prolapse. Rectocele Cystocele

Interventions

Intervention group: This study is performed among patients referred to Isfahan women's centers and hospitals. Women who have been diagnosed with rectocele, cystocele and uterine prolapse, etc., and ar
Are selected. Due to the immorality of depriving patients of treatment, it is not possible to select a control group. Sampling is done by available census. The researcher refers to the mentioned hospi
It is explained to the patients and in case of complete and informed consent, it is delivered to them and collected after completion. Patients undergo perineurography and posterior anterior repair (AP

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
25 Years to No maximum

Inclusion criteria

Inclusion criteria: Women with rectocele, cystocele and uterine prolapse candidate for perineural surgery and posterior anterior repair (APR) Satisfaction to enter the research

Exclusion criteria

Exclusion criteria: Exclusion of the subject from the study Lack of access to the subject to follow up

Design outcomes

Primary

MeasureTime frame
Body image. Timepoint: Before surgery and six months after surgery. Method of measurement: Questionnaire MBSRQ.;Sexual function. Timepoint: Before surgery and six months after surgery. Method of measurement: Questionnaire FSFI.

Secondary

MeasureTime frame
Quality of Life. Timepoint: Before surgery and six months after surgery. Method of measurement: questionnaire sf-36.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaryam Haj Hashemi

Esfahan University of Medical Sciences

hajhashemy73@yahoo.com+98 31 3236 7005

Outcome results

None listed

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