Clinical Study on the Effect of Acupuncture Combined with the Low-dose Progynova on Endometrial Receptivity of Thin Endometrium

Status

Recruiting

Phases

Phase 1

Study type

Interventional

Source

ITMCTR

Registry ID

ITMCTR1900000295

Enrollment

Unknown

Registered

2019-09-04

Start date

2019-06-01

Completion date

Unknown

Last updated

2023-02-20

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

Conditions

Thin Endometrium

Interventions

control group:4mg Progynova

treatment group:acupuncture+2mg Progynova

Eligibility

Sex/Gender

Female

Age

18 Years to 40 Years

Inclusion criteria

Inclusion criteria: (1) women in the age of 18-40 with fertility requirements;(2) menstruation occurs every 23-37 days, and mature follicles (18-25mm) can be discharged under b-ultrasound.(3) Sign the informed consent form.

Exclusion criteria

Exclusion criteria: (1) serious cardiovascular and cerebrovascular, liver, kidney, malignant tumor, hematopoietic system and mental diseases; (2) abnormal liver and kidney function; (3) have oral hormones or use contraceptives within three months; (4) history of acupuncture adverse reactions (such as acupuncture) and acupuncture contraindications (such as acupuncture site trauma).

Design outcomes

Primary

Measure	Time frame
endometial thickness;endometial thickness;	—

Secondary

Measure	Time frame
menstration;endometial type;endometrial blood flow;menstration;endometrial blood flow;E2;endometial type;E2;	—

Countries

China

Contacts

Public ContactChensi Zheng

595706965@qq.com+8613310830205

Outcome results

None listed

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