Actively Recruiting

Phase Not Applicable
Age: 20Years - 50Years
MALE
NCT07252518

Effect of Pentoxifylline + CoQ10 vs CoQ10 Alone on Sperm Motility in Subfertile Men With Asthenozoospermia

Led by Mst.Sumyara Khatun · Updated on 2025-11-26

56

Participants Needed

1

Research Sites

73 weeks

Total Duration

On this page

Sponsors

M

Mst.Sumyara Khatun

Lead Sponsor

B

Bangladesh Medical University

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this clinical trial is to learn if drug Pentoxifylline plus Coenzyme Q10 work to treat asthenozoospermia in subfertile male. It will also learn about the safety of drug Pentoxifylline plus Coenzyme Q10. The main questions it aims to answer are: Does drug Pentoxifylline plus Coenzyme Q10 increase the motility of sperm in participants? What medical problems do participants have when taking drug Pentoxifylline plus Coenzyme Q10 ? Researchers will compare drug Pentoxifylline plus Coenzyme Q10 combination to Coenzyme Q10 alone to see if drug Pentoxifylline plus Coenzyme Q10 combination works better. Participants will: Experimental Group:Pentoxifylline 400mg twice dailyand Coenzyme Q10 100mg twice daily for 3 months. Comparator Group: Coenzyme Q10 100mg twice daily for 3 months Visit the clinic after three months of treatment for checkups and tests

CONDITIONS

Official Title

Effect of Pentoxifylline + CoQ10 vs CoQ10 Alone on Sperm Motility in Subfertile Men With Asthenozoospermia

Who Can Participate

Age: 20Years - 50Years
MALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Subfertile men with asthenozoospermia (total motility 20% to less than 42%) according to WHO semen analysis, 2021
  • Age between 20 and 50 years
Not Eligible

You will not qualify if you...

  • Severe oligoasthenoteratozoospermia
  • Any medical, endocrine, or genetic disorders
  • History of chemotherapy or radiotherapy
  • Genital infection or genital surgery
  • Antioxidant supplementation in the last 3 months
  • Drug, alcohol, or substance abuse
  • Psycho-sexual abnormalities
  • Known hypersensitivity to xanthine-related products
  • Recent cerebral or retinal hemorrhage

AI-Screening

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Trial Site Locations

Total: 1 location

1

Bangladesh Medical University

Dhaka, Shahbag, Bangladesh, 1000

Actively Recruiting

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Research Team

M

Mst.Sumyara Khatun, MS

CONTACT

K

Kazi Jannatul Ferdouse, MBBS

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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