Asherman Syndrome

3

Review clinical trials related to Asherman Syndrome. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

CURENDO (Cord-blood Uterine Regeneration Endometrium): Platelet-rich Plasma Therapy Derived From Umbilical Cord Blood for the Treatment of Endometrial Pathologies (Asherman Syndrome / Endometrial Atrophy / Thin Endometrium)

In recent years, platelet-rich plasma (PRP) has emerged as a promising alternative for treating endometrial pathologies that affect the endometrial lining. Several studies have tested this therapeutic approach in human patients, but the results are inconclusive. Moreover, in recent years, different investigations have suggested that PRP derived from umbilical cord blood (hUC-PRP) contains a higher concentration of growth factors and other pro-regenerative molecules than PRP obtained from adult peripheral blood. In our previous pilot study conducted in 15 patients with endometrial atrophy/Asherman syndrome/thin endometrium, preliminary results indicate that hysteroscopic injection of hUC-PRP increases endometrial thickness and improves the endometrial pattern. For this reason, the present study aims to corroborate our previous findings by increasing the number of patients to 35, in prior HRT cycles in these women, to gain a deeper understanding of the effectiveness of this new therapy.

Participants needed: 35
Trial details
Age: 18-48Biological sex: FemaleType: InterventionalSponsor: Fundación IVIUpdated: Jul 13, 2026Locations: 1
Eligibility criteria

age between 18 and 48 years at the time of recruitment [+2]

Active genital infection at the time of recruitment [+7]

Status: Recruiting

Bone Marrow Derived Stem Cells Mobilization for Treatment of Abnormal Endometrium

This study will assess the use of autologous bone marrow stem cells mobilization using 1,1'-\[1,4-phenylenebis-(methylene)\]-bis-1,4,8,11-tetraazacyclotetradecane (PLERIXAFOR) as an effective medical therapy for the treatment of Asherman's Syndrome (AS), Atrophic Endometrium (AE) and Recurrent Implantation Failure (RIF).

Participants needed: 90
Trial details
Phase: Early Phase 1Age: 18-40Biological sex: FemaleType: InterventionalSponsor: Hugh TaylorUpdated: Nov 12, 2025Locations: 1
Eligibility criteria

Healthy, non pregnant females [+5]

Presence of hydrosalpinx (diagnosed by radiographic or ultrasound imaging) [+7]

Status: Not yet recruiting

Safety and Performance of the Semical Adhesion Barrier Gel for Prevention of Intra-uterine Adhesion

The aim of this study was to obtain short- and long-term performance and safety data of cross-linked hyaluronic acid-based adhesion barrier gel used to prevent intrauterine adhesion formation.

Participants needed: 80
Trial details
Age: 18+Biological sex: FemaleType: ObservationalSponsor: Semikal TechnologyUpdated: Sep 8, 2025Locations: 1
Eligibility criteria

Female patients aged 18 and over [+3]

Children and adolescents under 18 years of age [+8]