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PRP Prevents Recurrence of Intrauterine Adhesions (RPR-IUAs)

Y

Yanhong Deng

Status

Unknown

Conditions

Intrauterine Adhesion

Treatments

Procedure: gel
Procedure: Platelet-rich plasma

Study type

Interventional

Funder types

Other

Identifiers

NCT03629132
RPR-IUAs

Details and patient eligibility

About

Effect of platelet-rich plasma (PRP) on uterine scar fibrosis, endometrial receptivity and pregnancy outcome in patients with severe intrauterine adhesions

Full description

  1. Inclusion criteria: patients with intrauterine adhesions (AFS score >9 points); age 21 to 40 years old, with fertility requirements.
  2. Study design:prospective, randomized controlled cohort study, patients with intrauterine adhesions were randomized into two groups, the control group and the intervention group (intraoperative and postoperative 1 week postoperative PRP). The surgical procedures and postoperative medication regimens were the same.
  3. Compare the biochemical pregnancy rate, clinical pregnancy rate, abortion rate and live birth rate after hysteroscopic resection in PRP group and control group, and explore the effect of PRP on pregnancy outcome after intrauterine adhesion.

Enrollment

60 estimated patients

Sex

Female

Ages

20 to 37 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:Patients with intrauterine adhesions (AFS score >9 points); age 21 to 40 years old, with fertility requirements -

Exclusion Criteria:Endometrial tuberculosis, endometrial polyps, uterine submucosal fibroids, endometrial hyperplasia, endometrial malignant lesions, premature ovarian failure, chromosomal abnormalities

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Single Group Assignment

Masking

None (Open label)

60 participants in 2 patient groups

PRP
Experimental group
Description:
Platelet-rich plasma
Treatment:
Procedure: Platelet-rich plasma
Gel
Sham Comparator group
Description:
Self-crosslinking sodium hyaluronate gel
Treatment:
Procedure: gel

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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