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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05874518
Other study ID # LiuzhouMCHH
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 1, 2021
Est. completion date April 30, 2022

Study information

Verified date May 2023
Source Liuzhou Maternity and Child Healthcare Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To observe the effect of warm needling combined with electroacupuncture on the ovulation promotion rate and pregnancy rate in luteinized unruptured follicle syndrome (LUFS).


Recruitment information / eligibility

Status Completed
Enrollment 70
Est. completion date April 30, 2022
Est. primary completion date April 30, 2022
Accepts healthy volunteers No
Gender Female
Age group 23 Years to 48 Years
Eligibility Inclusion Criteria: - Infertility diagnosis criteria refer to the "Obstetrics and Gynecology" [10]: Infertility refers to the patient fails to conceive a pregnancy with normal sexual life and without contraception for 1 year. In primary infertility, pregnancy has never occurred. In secondary infertility, patients have previously conceived, but are unable to conceive again without contraception for 1 year. - The standard for ovulation infertility is formulated according to the first series of Guiding Principles for Clinical Research of New Chinese Medicine: Basal body temperature was continuously recorded for single phase for more than 3 months; Vaginal detached cell smear examination showed no significant periodic changes; Cervical mucus crystallization examination showed no periodic changes, and ellipsoid; There was no typical secretory period change in endometrial examination on 6 days before menstruation; a series of B-ultrasound monitoring showed no ovulation signs; Blood and urinary progesterone levels were lower than those in the luteal phase. Patients who met two of the above 6 items could be diagnosed with anovulation Exclusion Criteria: - Those who have any serious adverse reactions during the treatment process and cannot continue the treatment - Failing to follow the treatment plan and receiving other treatment - Patients who quit the treatment process by themselves, or who have an incomplete course of treatment, will have a negative effect on the curative effect

Study Design


Related Conditions & MeSH terms


Intervention

Other:
warm needling combined with electroacupuncture
Treatment begins on the 5th day of the menstrual cycle, qd (once a day), usually for 6-8 consecutive days, and continuing to the day of ovulation.
Drug:
The treatment with letrozole tablets was started on the fifth day of the menstrual cycle
Letrozole tablets were given at 2.5mg (Jiangsu Hengrui Pharmaceutical Co., Ltd., H19991001, 2.5mg per tablet), po (oral), qd, for 5-7 consecutive days. When the diameter of follicles reaches 18mm, Chorionic gonadotrophin is given at 5000u (Lizhu Group Lizhu Pharmaceutical Factory, Chinese medicine H44020668, 5000u per branch), with intramuscular injection, qd, to promote follicle discharge. Patients were also instructed to have sexual intercourse on the same day and on day 2.

Locations

Country Name City State
China Fanghua Yang Liuzhou Guangxi

Sponsors (1)

Lead Sponsor Collaborator
Liuzhou Maternity and Child Healthcare Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Ultrasound characteristics of ovulation Monitoring follicular intima thickness About 10 days on average until =18mm follicle disappears or 20mm follicle volume decreases
Primary vaginal B-ultrasound to monitor follicles (size and discharge) and endometrial thickness on the fifth day of menstruation vaginal B-ultrasound to monitor follicles (size and discharge) and endometrial thickness on the fifth day of menstruation the endometrium of =8mm on the fifth day of menstruation
Primary Use vaginal B-ultrasound to monitor follicles (size and discharge) and endometrial thickness on the fifth day of menstruation When the follicle size reached 18mm and Chorionic gonadotrophin was injected 48 hours after chorionic gonadotropin injection
Primary Pregnancy judgment Pregnancy was determined by detecting serum HCG (human chorionic gonadotropin) 14 days after ovulation 14 days after ovulation
Primary Pregnancy judgment At about 50 days of pregnancy, pregnancy sac or fetal heart beat through vaginal B ultrasound about 50 days of pregnancy
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