Prevalence of Sexual Dysfunction After Rectal Surgery and Patient Satisfaction of Preoperative Discussions

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

16 participants

Study Classification

OBSERVATIONAL

Study Start Date

2015-08-31

Study Completion Date

2019-05-31

Brief Summary

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Sexual dysfunction after rectal surgery varies widely in the literature. Prevalence of sexual dysfunction before surgery and desire of patient to treat this condition is also not well established.

Objectives of this prospective cohort study were to determine prevalence of sexual dysfunction with a questionnaire before and after surgery. Patient's satisfaction and quality of life were also collected regarding preoperative information given.

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Detailed Description

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Conditions

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Sexual Dysfunction Rectal Surgery Patient Satisfaction

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Interventions

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rectal surgery

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Male between 18 and 65 years old
* Will undergo one of the following surgeries in the 12 months after the initial visit:

* Low anterior resection
* Abdominoperineal resection with end colostomy
* Total proctocolectomy with ileostomy
* Total proctocolectomy with ileoanal reservoir
* Proctectomy
* Having had a sexual intercourse in the 4 weeks prior to the initial visit
* Having the desire to maintain sexual activities in the post-operative period

Exclusion Criteria

* Tadalafil allergy/hypersensitivity
* Having received treatment for erectile dysfunction or medical treatment in the 4 weeks prior to the initial visit
* Active consumption of nitrate derivatives (NO)
* History of non-arteritic ischemic optic neuropathy
* Severe renal or hepatic insufficiency
* Stroke in the last 6 months
* Myocardial infarction in the last 3 months
* Unstable angina pectoris or angina pectoris during sexual relations
* Cardiac insufficiency Class ≥ 2 in the last 6 months
* Uncontrolled arrhythmia, hypotension or hypertension

Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

MALE

Accepts Healthy Volunteers

Yes