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

A Multi-center, Randomized, Single-blind, Controlled Clinical Trial of Treatment of Severe Asherman Syndrome by Collagen Scaffold Loaded With Autologous Bone Marrow Mononuclear Cells

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.

Study Overview

• Status: Completed
• Conditions: Infertility; Asherman Syndrome
• Intervention / Treatment: Device: collagen/ABMNC scaffold; Device: Foley catheter balloon

Detailed Description

Severe asherman syndrome will lead to infertility, and the most common method to treat asherman syndrome is operating to dissect adhesions. In order to prevent the postoperative re-adhesion, many physical isolation measures have been tried. However, they don't improve the microenvironment of endometrial regeneration. It's reported that bone marrow mononuclear cells have good effects on the functional recovery of injured uterus. This study will determine whether collagen scaffolds loaded with autologous bone marrow mononuclear cells will be more effective than Foley balloon catheters at treating infertile women with severe intrauterine adhesions who have taken hysteroscopic adhesiolysis. In addition, the study will be carried out in 2 centers, one is the Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School, the other is Changzhou Maternal and Child Health Care Hospital that is in Jiangsu Province.

• Study Type: Interventional
• Enrollment (Actual): 152
• Phase: Not Applicable

Contacts and Locations

Study Locations

• China
  • Jiangsu
    • Nanjing, Jiangsu, China, 210008
      • Nanjing Drum Tower Hospital

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 20 years to 40 years (ADULT)
• Accepts Healthy Volunteers: Yes
• Genders Eligible for Study: Female

Description

Inclusion Criteria:

• Having a clear desire to fertility;
• Infertility that is defined as a women fails to become pregnant after having a normal sex life for two years without contraception.
• Hysteroscopy examination confirmed intrauterine adhesions(patients who has at least one of the three symptoms which are amenorrhea, hypomenorrhea or infertility, and hysteroscopy or histologic diagnosis of intrauterine adhesions), meeting American Fertility Society diagnostic criteria Ⅱ-III;
• Normal ovarian function;
• Regular Menstrual cycles and menstruation is normal before abortion or curettage;
• BMI< 30 kg/m2;
• Sign a consent form;
• Follow the test plan and follow-up process.

Exclusion Criteria:

• Hereditary diseases;
• Simple thin endometrium with no uterine cavity adhesion;
• Simple Uterine scar formation with no uterine cavity adhesion after hysteroscopic adhesiolysis;
• Contraindications to bone marrow collection or assisted reproductive technology;
• History of malignant tumor;
• Other diseases associated with the uterus: uterine fibroids, severe adenomyosis, severe malformations of the uterus;
• Abnormal blood coagulation, liver and kidney dysfunction, or other diseases which the researchers think may affect the study(such as: uncontrolled hypertension, diabetes, sexually transmitted diseases);
• With a positive urine pregnancy test；
• Participating in other clinical studies at the same time;
• Hysteroscopic adhesiolysis more than 3 times in the past.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: TREATMENT
• Allocation: RANDOMIZED
• Interventional Model: PARALLEL
• Masking: SINGLE

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
EXPERIMENTAL: collagen/ABMNC scaffold; collagen/ABMNC scaffold covered on Foley catheter balloon inserted after hysteroscopic adhesiolysis	Device: collagen/ABMNC scaffold; The patients will receive a bone marrow puncture to collect bone marrow cells which are used to isolation of ABMNCs. After that, hysteroscopic adhesiolysis will be done according to the patient's uterine adhesion. Then, the collagen/ABMNCs scaffold was covered on a Foley catheter balloon and placed into the uterine cavity. The catheter balloon was kept for 24 hours and then removed. Oral antibiotics were given to prevent infection in the second and third days after operation. 72 hours after the surgery, a vaginal speculum examinations will be done in order to make patients unknown about their arms. Estrogen will be administrated for 3 cycles to support the endometrial regeneration after the surgery. The clinical follow up will be done at 1, 3 and 6 months after the procedure.
ACTIVE_COMPARATOR: Foley catheter balloon; Foley catheter balloon inserted after hysteroscopic adhesiolysis	Device: Foley catheter balloon; The patients will receive a sham bone marrow puncture which just has a local anesthesia and collects no bone marrow cells to isolation. After that, hysteroscopic adhesiolysis will be done according to the patient's uterine adhesion. And then, a Foley catheter balloon will be placed into the uterine cavity and kept for 72 hours before it is removed. Oral antibiotics were given to prevent infection in the second and third days after operation. Estrogen will be administrated for 3 cycles to support the endometrial regeneration after the surgery. The clinical follow up will be done at 1, 3 and 6 months after the procedure.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Ongoing pregnancy rate	A successful clinical pregnancy means that at the 12th week of pregnancy, ultrasound reveals that the fetus had a heart activity and the size of the fetus is in consistent with the gestational week.	up to 24 months

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Menstrual volumes and menstrual improvement:	PBAC scores in the third and sixth menstrual cycles after the initial adhesiolysis and PBAC scores increase compared to pre-operation	at 3 and 6 months post-operation
Maximal endometrial thickness	Measure the endometrial thickness during ovulation by ultrasound by the same trained medical sonographers at 3 and 6 months after surgery, comparing with pre-operation.	at 3 and 6 months post-operation
Re-adhesion rate at the second-look hysteroscopy		at 3 months post-operation
AFS score at the second-look hysteroscopy and AFS score decrease compared to pre-operation		at 3 months post-operation
Miscarriage rate		up to 24 months
preterm birth rate		up to 24 months
ectopic pregnancy rate		up to 24 months
live birth rate		up to 24 months

Collaborators and Investigators

• Sponsor: The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School
• Collaborators: Changzhou Maternal and Child Care Hospital
• Investigators: Principal Investigator: Yali Hu, MD,PhD, The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School

Study record dates

Study Major Dates

• Study Start (ACTUAL): February 22, 2016
• Primary Completion (ACTUAL): July 22, 2022
• Study Completion (ACTUAL): July 22, 2022

Study Registration Dates

• First Submitted: January 30, 2016
• First Submitted That Met QC Criteria: February 8, 2016
• First Posted (ESTIMATE): February 11, 2016

Study Record Updates

• Last Update Posted (ACTUAL): November 30, 2022
• Last Update Submitted That Met QC Criteria: November 24, 2022
• Last Verified: November 1, 2022

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Pathologic Processes; Disease; Syndrome; Infertility; Gynatresia
• Other Study ID Numbers: 201600301

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: YES
• IPD Plan Description: Both the study protocol and the statistical analysis plan are available on request.
• IPD Sharing Time Frame: The data are available on reasonable request beginning 3 months and ending 5 years following article publication.
• IPD Sharing Access Criteria: Researchers who provide a methodologically sound proposal will be given access to the data to achieve aims in the proposal.
• IPD Sharing Supporting Information Type: STUDY_PROTOCOL; SAP