Evaluation of Marital and Sexual Satisfaction of Wives to Erectile Dysfunction Males

January 24, 2017 updated by: Ahmad Raef Sadek, Adam International Hospital

Evaluation of Marital and Sexual Satisfaction of Wives to Erectile Dysfunction Males Using Intra Corporeal Injection (Ici). In Correlation to Personality Profile

Erectile Dysfunction (ED), previously known as sexual impotence, is defined as the persistent inability to obtain and/or maintain a penile erection that is hard enough for satisfactory sexual intercourse. The number of reported patients with ED is increasing and it is becoming a real medical problem.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Marital satisfaction is a global evaluation of the state of one's marriage or current long-term romantic relationship. This global evaluation can be a reflection of a how happy people are in their marriage in general or a composite of satisfaction with several specific facets of the marital relationship. Sexual health can be described as enjoying and fulfilling sexual desires without harming, physical or psychological, oneself or others. Sexual functioning is an important part of a patient's health and well-being. Patients often seek for treatment late due to embarrassment and commonly with an alternative problem. Sexual and erectile functions are considered important components of men's overall health. The psychosocial impact of ED can lead to depression, loss of self-esteem, and relationship and marital difficulties. Personality is defined as the "distinctive and characteristic patterns of thought, emotion and behavior that define an individual's personal style and influence his or her interaction with the environment".

Study Type

Observational

Enrollment (Actual)

70

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 50 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Males complaining of erectile dysfunction.

Description

Inclusion Criteria:

  • Married couples

Exclusion Criteria:

  • Unmarried couples.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Case-Control
  • Time Perspectives: Prospective

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Erectile dysfunction patients
Questionnaire sheets.
Other: Questionnaire sheets

A- Marital satisfaction Index (MSI). Interview (Modified Arabic translation)

B- Sexual Satisfaction Scale:(SSS). The Arabic version of the sexual satisfaction scale was used.

C- International Index of Erectile Function Questionnaire (IIEF-5): For male subjects.

D- The Eysenck Personality Questionnaire (EPQ):

The Arabic version of the EPQ was used.
Normal males
Questionnaire sheets.
Other: Questionnaire sheets

A- Marital satisfaction Index (MSI). Interview (Modified Arabic translation)

B- Sexual Satisfaction Scale:(SSS). The Arabic version of the sexual satisfaction scale was used.

C- International Index of Erectile Function Questionnaire (IIEF-5): For male subjects.

D- The Eysenck Personality Questionnaire (EPQ):

The Arabic version of the EPQ was used.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Marital and sexual satisfaction.
Time Frame: Six months.
Questionnaire sheets.
Six months.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Adam International Hospital

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 1, 2014

Primary Completion (Actual)

June 1, 2014

Study Completion (Actual)

June 30, 2014

Study Registration Dates

First Submitted

January 22, 2017

First Submitted That Met QC Criteria

January 24, 2017

First Posted (Estimate)

January 26, 2017

Study Record Updates

Last Update Posted (Estimate)

January 26, 2017

Last Update Submitted That Met QC Criteria

January 24, 2017

Last Verified

January 1, 2017

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 2014 (U.S. NIH Grant/Contract)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

Yes

IPD Plan Description

Contact the authors

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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