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Homeopathic medicines for treatment of erectile problems

Phase 2
Conditions
Health Condition 1: N521- Erectile dysfunction due to diseases classified elsewhere
Registration Number
CTRI/2023/03/050318
Lead Sponsor
D N De Homoeopathic Medical College and Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1. Patients suffering from ED (ICD10-Code N52).

2. Male Patients aged between 18 and 65 years.

3. Literate patients; ability to read English and/or Bengali and/or Hindi. Illiterate people will be interviewed by the investigators maintaining adequate privacy to fill up the scales or questionnaires.

4. Providing written informed consent voluntarily.

Exclusion Criteria

1. Vulnerable population - unconscious, non-ambulatory, too sick for consultation, differently abled, terminally ill or critically ill patients, and mentally incompetent people.

2. Diagnosed cases of unstable mental or psychiatric illness or other uncontrolled diabetes or life-threatening illness affecting the quality of life or any organ failure.

3. Patient with a habit of tobacco chewing and/or smoking, alcoholism and/or any other form(s) of substance abuse and/or dependence.

4. History of significant injury to the lower back or any other spinal injury followed by erectile dysfunction

5. Self-reported immune-compromised state.

6. Already undergoing homoeopathic treatment for chronic disease or any other mode of treatment for ED within the last 6 months.

7. Simultaneous participation in any other clinical trials.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
International Index of Erectile Function (IIEF)Timepoint: At baseline, and every month, up to 3 months of intervention
Secondary Outcome Measures
NameTimeMethod
Male Sexual Health QuestionnaireTimepoint: At baseline, and every month, up to 3 months of intervention;Measure Yourself Medical Outcome Profile v2 (MYMOP-2) questionnaireTimepoint: At baseline, and every month, up to 3 months of intervention
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