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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT03817827
Other study ID # 123
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated
Start date May 5, 2018
Est. completion date June 30, 2019

Study information

Verified date August 2021
Source National Research Centre, Egypt
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The present study will be designed to investigate the effect of acupuncture and diet modification using soy products on amenorrhea in female athlete triad. For this purpose this study will be carried out on sixty female athletes participating gymnastics. They will be recruited from Sports Medicine specialized center in Nasr City, their ages will range from 17 to 25 years old and their BMI will be < 20 Kg/m2 .


Description:

The subjects will be divided into three groups equal in number, matched for measured variable: Group (A): Acupuncture only will be used in this group for 30 minutes, three times per week for twelve weeks. The acupuncture needles were inserted in points located on the abdomen. Group (B): This group will receive only the diet modification contains soy products (phytoestrogen) as 100 milliliter soy milk and 100 grams soy beans daily in the morning as a breakfast alone to ensure its absorption, this dose had been taken for 12 weeks. Group (C): This group will receive both acupuncture therapy for 30 minutes, three times per week for 12 weeks and diet modification contains soy products as 100 milliliter soy milk and 100 grams soy beans daily in the morning for 12 weeks.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date June 30, 2019
Est. primary completion date March 5, 2019
Accepts healthy volunteers No
Gender Female
Age group 17 Years to 25 Years
Eligibility Inclusion Criteria: - All patients suffering from athletic amenorrhea. - Their age will be ranged from 17-25 years old. - Their body mass index will be less than 18.5 kg/m2. - No history of previous pregnancies. - No history of any pathological disease causing amenorrhea. - They are medically stable and consented to participate in the study. Exclusion Criteria: - Patients with gynecological diseases that may cause amenorrhea. - Patients using contraceptive pills. - Patients using hormonal treatment. - Patients using induction of ovulation methods. - Patients following any other diet modification method. - Patients who receive any drug with side effect of amenorrhea.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Acupuncture
this group will receive Acupuncture for 30 minutes three times per week
Dietary Supplement:
Diet supplementary
Diet supplementary with soy product

Locations

Country Name City State
Egypt Sports medicine speciaized center Cairo Nasr City

Sponsors (1)

Lead Sponsor Collaborator
National Research Centre, Egypt

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary follicle stimulating hormone Blood sample will be taken from the patient at the beginning of the study and three months later to determine the change of hormone level using Immulite 1000 immunoassay analyzer three months
Primary Luteinizing hormone Blood sample will be taken from the patient at the beginning of the study and three months later to determine the change of hormone level using Immulite 1000 immunoassay analyzer three months
Primary estradiol 2 Blood sample will be taken from the patient at the beginning of the study and three months later to determine the change of hormone level using Immulite 1000 immunoassay analyzer three months
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