testing a Unani Herbal Remedy for safety and Effectiveness in Testing Premature ejaculation

A SINGLE BLIND,CLINICAL TRIAL TO EVALUATE THE SAFETY AND EFFICACY OF COMPOUND UNANI FORMULATION IN THE MANAGEMENT OF SUR AT-E-INZAL(PREMATURE EJACULATION) - NIL

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/11/076234

Enrollment

Registered

2024-11-04

Start date

Unknown

Completion date

Unknown

Last updated

2024-11-11

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

Conditions

Health Condition 1: N531- Ejaculatory dysfunction

Interventions

Intervention1: Unani Formulation of Tukhm e Kahu Tukhm e kharfa Aspagol Nilofer Kafoor Dhaniya Gulnar: Tukhm e Kahu(30gm) Tukhm e kharfa(30gm) Aspagol(10.5gm) Nilofer(7mg) Kapoor(1092mg) Dhaniya(10.

Eligibility

Inclusion criteria

Inclusion criteria: All socio economic status Married

Exclusion criteria

Exclusion criteria: Unmarried patients Patient less than 21 year and above 45 years of age User of antidepressants Patients suffering from Diabetes mellitus ,CAD, TB Patients suffering from STD, Prostitis, urethritis Major endocrinal disorder like hypothyroidism and other pathology Patient with erectile dysfunction

Design outcomes

Primary

Measure	Time frame
Improvement in EjaculationTimepoint: Patient will be access on 0day 20day	—

Secondary

Measure	Time frame
Ejaculation with own and partner’s satisfaction Number of penile thrust 25 Enjoyment in every sex act Timepoint: Patient will be access to 0 day 10 day and 20 day	—

Countries

India

Contacts

Public ContactSHARIK Imran A Rafique

Government Nizamia Tibbi college and General Hospital charminar Hyderabad

dr.faroqui@gmail.com9849139356

Outcome results

None listed

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