A Survey and Clinical Study of Ayurvedic formulations and Psycho-therapy in the management of Manas Klaibya (Psychological impotence) in Male ParticipantsÃ¢â?¬?

An Etiopathological Study of Manas Klaibya (Psychological impotence) With Randomized Controlled Clinical Trial of Guduchyadi Rasayana, Vidarikanda Churna and Sattvavajaya Chikitsa (Psycho-therapy) in Male Participants

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2022/09/045610

Enrollment

120

Registered

2022-09-16

Start date

Unknown

Completion date

Unknown

Last updated

2022-10-17

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

Conditions

Health Condition 1: N521- Erectile dysfunction due to diseases classified elsewhere

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients suffer with classical sign and symptoms of Manas Klaibya (Psychological impotence). 2. Patients having scoring less than 21 with International Index of Erectile Dysfunction (IIEF-5) questionnaire (SHIM). 3. Patients willing to give written informed consent

Exclusion criteria

Exclusion criteria: 1. Patients having other history of systemic pathology like Tuberculosis, Renal failure, Diabetes Mellitus, Hypertension, severe urinary tract infections, Urethral stricture and malignancy of urogenital system etc. 2. Patients having congenital deformity of urogenital tract and structural abnormalities

Design outcomes

Primary

Measure	Time frame
To understanding the etiopathogenesis and evaluate the efficacy of Guduchyadi Rasayana, Vidarikanda Churna and Sattvavajaya Chikitsa (Psycho-therapy) in Manas Klaibya (Psychological impotence) of male participants. Timepoint: 60 days	—

Secondary

Measure	Time frame
1. To assess changes in Serum Testosterone (Total) level before and after Intervention b/w day 0 and day 60. 2. To assess changes in International Index of Erectile Function (IIEF-5) Score before and after intervention i.e b/w day 0 and day 60. 3. To assess the changes in Sexual Quality Of Life Questionnaire (SQLQ) before and after intervention i.e b/w day 0 and day 60Timepoint: 60 Days.	—

Countries

India

Contacts

Public ContactDr Surendra Kumar Sharma

National Institute of Ayurveda Deemed to be University (De novo)

drsksm31@rediffmail.com9414361874

Outcome results