Clinical Trials Logo

Asherman Syndrome clinical trials

View clinical trials related to Asherman Syndrome.

Filter by:

NCT ID: NCT03249415 Recruiting - Asherman Syndrome Clinical Trials

Use of PRP in Endometrial Reconstruction

Start date: July 18, 2017
Phase:
Study type: Observational

Infertility, which affected 48.5 million couples worldwide in 2010 alone, has many causes; some causes result from issues related to the endometrium. Unfortunately, no cure exists for medical conditions resulting in the destruction of the endometrium, or for non-functional uterus. Thus, safe and effective therapies are needed to treat these diseases and to establish fertility in affected women. These novel techniques refer to the use and application of regenerative/paracrine factors to regenerate the endometrium in patients with Asherman's Syndrome (AS) and Endometrial Atrophy (EA).These new therapies based on the injection of the identified regenerative/paracrine factors and the platelet-rich plasma (PRP) from whole blood in an immunodeficient mouse model with AS/EA, evaluating their contribution and/or effect in the endometrial repair by functional proofs.

NCT ID: NCT03166189 Completed - Infertility, Female Clinical Trials

Autologous Bone Marrow-derived Mesenchymal Stem Cells for Atrophic Endometrium in Patients With Repeated IVF Failures

Start date: December 20, 2017
Phase: Phase 2
Study type: Interventional

Investigators will examine safety and efficiency of the cell product of autologous bone marrow-derived mesenchymal stem cells (MSC) for patients with repeated IVF failures and hypoplastic or/and fibrosis process of endometrium

NCT ID: NCT02867202 Completed - Asherman Syndrome Clinical Trials

Adjuvant Therapy for Intrauterine Adhesions Between Two Groups

Start date: June 2015
Phase: N/A
Study type: Interventional

This study was taken out to compare two mechanical devices (intrauterine balloon and Intrauterine Contraceptive Device Plus Foley Catheter) in the therapy for intrauterine adhesions after hysteroscopic adhesiolysis. Participates were assigned into two groups by randomly.

NCT ID: NCT02746679 Completed - Asherman Syndrome Clinical Trials

Impact of Mindfulness Based Stress Reduction on Anxiety, Depression and QOL in Women With Intrauterine Adhesion.

IMBSRADQWIUA
Start date: January 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether mindfulness based stress reduction are effective on improve anxiety, depression and quality of life in women with intrauterine adhesion

NCT ID: NCT02726971 Completed - Asherman Syndrome Clinical Trials

Comparison of Different Doses of Oestrogen Therapy for Preventing Intrauterine Adhesion

Start date: April 2016
Phase: Phase 1/Phase 2
Study type: Interventional

This single-center,prospective,randomized,controlled trial is conducted to evaluate the efficacy of different doses of estrogen artificial periodic therapy after hysteroscopic adhesiolysis in patients with moderate-severe adhesion.

NCT ID: NCT02680366 Completed - Infertility Clinical Trials

Treatment of Severe Asherman Syndrome by Collagen Scaffold Loaded With Autologous Bone Marrow Mononuclear Cells

Start date: February 22, 2016
Phase: N/A
Study type: Interventional

This study evaluates the addition of collagen scaffold loaded with autologous bone marrow mononuclear cells(ABMNC) to Foley catheter balloon after hysteroscopic adhesiolysis in the treatment of severe asherman syndrome. Half of participants will receive collagen/ABMNC scaffold after hysteroscopic adhesiolysis, while the other half will receive Foley catheter balloon.

NCT ID: NCT01637974 Recruiting - Uterine Myoma Clinical Trials

Efficiency of INTERCOAT (Oxiplex/AP Gel) in Preventing Intrauterine Adhesion Formation in Hysteroscopic Surgery

Start date: December 2012
Phase: N/A
Study type: Interventional

The study purpose is to examine the influence of INTERCOAT in prevention of intra-uterine adhesions formation after any hysteroscopic surgery.

NCT ID: NCT01377779 Completed - Asherman Syndrome Clinical Trials

Efficiency of Intercoat (Oxiplex/AP Gel)in Decreasing Intrauterine Adhesions

Start date: September 2009
Phase: N/A
Study type: Interventional

This is a prospective single blind randomized controlled pilot study was designed to investigate whether the biological barrier Intercoat (Oxiplex/AP gel) reduces formation of intrauterine adhesions following hysteroscopic treatment for retained products of conception.