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Effect of bupropion tablets compared to sildenafil tablets and Ginseng on sexual function (erectile dysfunction) in men with type 2 diabetes who were referred to endocrinology clinic of Vali Asr Hospital of Zanjan.

Compare the Efficacy of Bupropion tablets with sildenafil tablet and Ginseng in sexual function in men with type 2 diabetes with erectile dysfunction.

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016111819554N11
Enrollment
80
Registered
2016-12-11
Start date
2016-04-20
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Sexual dysfunction. Male erectile dysfunction, unspecified

Interventions

Intervention 1: 20 patients: Bupropion Tab(150mg)for 10 weeks. Intervention 2: 20 patients: Sildenafil Tab(50mg)for 10 weeks. Intervention 3: 20 patients: Ginseng capsule for 10 weeks. Intervention 4:
Treatment - Drugs
Treatment - Other
Placebo
20 patients: Bupropion Tab(150mg)for 10 weeks
20 patients: Sildenafil Tab(50mg)for 10 weeks.
20 patients: Ginseng capsule for 10 weeks

Sponsors

Zanjan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
30 Years to 80 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: age between 30-80 years ild; sexual dysfunction from 6 month ago; no relationship problems with partner from 6 month ago; HbA1c less than 10 & FBS less than 200 from 6 month ago; normal serum testosterone and prolactine levels; non-interference in the our drugs with prescription medications; no history of priapism. Exclusion criteria: the anatomical penile dysfunction; history of prostatectomy; sever hematologic & renal &liver dysfunction; Nitrate consumption; coronary artery disease; blood pressure more than 170/100 or less than 90, proliferative retinopathy; autonomic neuropathy; ketoacidosis history in 2 years ago; tachycardia.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Erectile dysfunctions. Timepoint: first day and 10 weeks later. Method of measurement: IIEF-5 standard questionnaire.;Serum colestrol level. Timepoint: first day. Method of measurement: laboratory kits (Calorimetry enzimatic).;Serum triglyceride level. Timepoint: first day. Method of measurement: laboratory kits (Calorimetry enzimatic).;Serumfasting blood sugar level. Timepoint: first day. Method of measurement: laboratory kits (Calorimetry enzimatic).;HbA1c. Timepoint: first day. Method of measurement: laboratory kits.;Serum prolactin level. Timepoint: first day. Method of measurement: laboratory kits (elisa).;Serum Testosterone level. Timepoint: first day. Method of measurement: laboratory kits (elisa).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Maryam Jameshorani

Zanjan University of Medical Sciences

dr.shirinjameshorani@yahoo.com+98 24 3377 0814

Outcome results

None listed

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