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A Clinical Study to check the effect and Safety of Sildenafil Citrate plus Dapoxetine Tablets for the treatment of co-existing Erectile Dysfunction and Premature Ejaculation.

A Phase-III, Multicentric, Randomized, Double Blind, Placebo-Controlled, Comparative Clinical Study to Evaluate the Efficacy and Safety of Sildenafil Citrate 50 mg plus Dapoxetine 60 mg Tablet and Sildenafil Citrate 100 mg plus Dapoxetine 60 mg Tablet in the treatment of co-existing Erectile Dysfunction and Premature Ejaculation.

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/12/011017
Enrollment
399
Registered
2017-12-28
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- Erectile Dysfunction and Premature Ejaculation Health Condition 2: N528- Other male erectile dysfunction

Interventions

Intervention1: Sildenafil Citrate 50 mg plus Dapoxetine 60 mg Tablet, Sildenafil Citrate 100 mg plus Dapoxetine 60 mg Tablet : One Tablet taken orally with water, as needed, approximately 1 hour prior

Sponsors

Ajanta Pharma Ltd
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Male subjects between 21 to 64 years of age both inclusive. 2.Subjects with known case of co-existing Erectile Dysfunction and Premature Ejaculation who are not on any of the treatment for this condition for last 7 days. 3.Male subjects with stable, monogamous, heterosexual relationship for at least 6 months and expected/planned to maintain this relationship for duration of study. 4.Penile Doppler standard systolic and diastolic velocity range for inclusions ( 5.Subjects meeting with diagnostic criteria for erectile dysfunction (as per the international index of erectile function (IIEF) score lesser than or equal to 21). 6.Subjects meeting with diagnostic criteria for Premature Ejaculation (PE score greater than or equal to 11). 7.Subjects with intravaginal ejaculatory latency time (IELT) of 8.Subject and his partner agreeing to attempt sexual intercourse at least 2 times/week. 9.Subjects who are willing to sign informed consent for participation in the study and willing to adhere to all protocol procedures.

Exclusion criteria

Exclusion criteria: 1.Previous events or other conditions associated with premature ejaculation/erectile dysfunction including but not limited to spinal trauma or pelvic surgery. 2.Subjects with genital anatomical deformities including but not limited to penile deformities. 3.Sexual dysfunction in female partner, painful intercourse, partners with decreased interest in intercourse or other forms of sexual dysfunction. 4.Subjects with known case of psychiatric illness or previous suicidal attempts. 5.Subjects with known case of Epileptic seizures. 6.Subjects with known case of stroke, myocardial infarction, heart failure, unstable angina and cardiac arrhythmias. 7.Subjects with abnormal Liver Function Test with (LFT) values more than 2.5 times the upper limit of normal. 8.Subjects with abnormal eGFR ( 9.Subjects with Type 1 Diabetes will be excluded from the study. 10.Subjects with Type 2 Diabetes Mellitus whose diabetes has not been stable and uncontrolled for the previous three months and with HbA1C value greater than 8 mmol/mol will be excluded from the study.

Design outcomes

Primary

MeasureTime frame
â?¢ To evaluate the efficacy of Sildenafil Citrate 50mg plus Dapoxetine 60mg Tablets and Sildenafil Citrate 100mg plus Dapoxetine 60mg Tablets in the treatment of co-existing Erectile Dysfunction and Premature Ejaculation.Timepoint: At the end of 12 week

Secondary

MeasureTime frame
â?¢ To evaluate the safety of Sildenafil Citrate 50mg plus Dapoxetine 60mg Tablets and Sildenafil Citrate 100mg plus Dapoxetine 60mg Tablets in the treatment of co-existing Erectile Dysfunction and Premature Ejaculation.Timepoint: At the end of 12 week

Countries

India

Contacts

Public ContactDr Shailesh Singh

Ajanta Pharma Ltd

shailesh.singh@ajantapharma.com0226062111

Outcome results

None listed

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