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Cryopreservation Medium With Apigenin on Post-thaw Human Sperm

C

Chulalongkorn University

Status

Completed

Conditions

Healthy

Treatments

Dietary Supplement: Apigenin

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The goal of this clinical trial is to compare the effect of apigenin supplementation in freezing medium with no apigenin supplementation in freezing medium on post-thaw human sperm motility. It will also evaluate the sperm viability, total antioxidant capacity, and oxidative stress markers. The main questions it aims to answer are:

  • Does apigenin supplementation in freezing medium improve the post-thaw sperm motility?
  • Does apigenin supplementation in freezing medium improve the post-thaw sperm viability, total antioxidant capacity, and oxidative stress?

Full description

All normal semen samples from participants who give written informed consent and meet the eligibility requirements will be included in the study. Prepared semen samples were divided into 3 groups.

  1. Pre-freezing sperm suspension
  2. Frozen-thawed control without apigenin supplementation in freezing medium
  3. Frozen-thawed sperm suspension with apigenin 0.2 mM supplementation in freezing medium Baseline sperm motility will be measured in pre-freezing sperm suspension. The last 2 groups will be stored in liquid nitrogen for at least one week. After thawing, the sperm suspensions will be evaluated for motility, viability, total antioxidant capacity, and oxidative stress markers.

Enrollment

57 patients

Sex

Male

Ages

18 to 45 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Healthy men aged 18-45 years who can receive semen analysis services at the Reproductive Biology Unit, Chulalongkorn Hospital, Thai Red Cross Society
  • Normal semen analysis results according to the World Health Organization criteria (Volume ≥ 1.4 mL, Sperm concentration ≥ 16 million/mL, Total motility ≥ 42%, Progressive motility ≥ 30%)
  • Giving consent

Exclusion criteria

  • A history of accidents, radiation to the testes, or a history of male reproductive system surgery
  • Undescended testis
  • Varicocele
  • A history of taking certain medications that affect sperm production, such as chemotherapy, hormones
  • Currently having sexually transmitted disease

Trial design

Primary purpose

Supportive Care

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

57 participants in 2 patient groups

Control
No Intervention group
Description:
Frozen-thawed sperm suspension without apigenin supplementation in freezing medium
Apigenin
Experimental group
Description:
Frozen-thawed sperm suspension with apigenin 0.2 mM supplementation in freezing medium
Treatment:
Dietary Supplement: Apigenin

Trial contacts and locations

2

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Central trial contact

Punyawee Utaipatanacheep; Porntip Sirayapiwat

Data sourced from clinicaltrials.gov

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