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Teatment of Premature Ejaculation with Safuf Aslasoos a Unani poly-herbal formula

Therapeutic evaluation of effect of Polyherbal formulation Safuf Aslasoos in Surat al Inzal Premature Ejaculation: A Randomized Double Blind Placebo Controlled Clinical Trial - Nil

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/07/070104
Enrollment
40
Registered
2024-07-05
Start date
Unknown
Completion date
Unknown
Last updated
2024-07-22

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: Poly-herbal formulation Safuf Aslasoos: The ingredients of Safuf Aslasoos is Aslasoos (50g), Tukhm sudab (130g), Tukhm sambhalu (130g), Tukhm kahu (75g), Gulnar (100g), and Gul surkh (1

Sponsors

Luqman Unani Medical College Hospital and Research Centre
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Gender: Male Age:21 - 47 years Only married men without any obvious organic cause of PME IVELT score 2 or greater

Exclusion criteria

Exclusion criteria: Diagnosed patients, those having organic cause like anatomical abnormalities, Genital infection, and Neurological disorder Patients with Erectile Dysfunction Patients with known case of psychological and psychiatric disease Patients with immunosuppressive disease/drugs Alcohol and drug abuse Non –compliance to the trial protocol

Design outcomes

Primary

MeasureTime frame
Intra -Vaginal Ejaculatory Latency Time (IVELT) Index of Premature Ejaculation (IPE) Premature Ejaculation Diagnostic Tool (PEDT) Timepoint: Baseline, fourteenth day and after trial

Secondary

MeasureTime frame
Premature Ejaculation Profile (PEP) International Index of Erectile Function (IIEF)Timepoint: Before and After trial

Countries

India

Contacts

Public ContactDr Khaleel Ahmed Hungund

Luqman Unani Medical College Hospital and Research Centre

drmqkhan@yahoo.com9849438319

Outcome results

None listed

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