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Efficacy and Safety of Crosslinked Hyaluronan Gel for Preventing Intrauterine Adhesion

Primary Purpose

Intrauterine Adhesion

Status
Completed
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Crosslinked hyaluronic acid gel
Foleys balloon catheter
Sponsored by
Xiaozheng Shu
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Intrauterine Adhesion focused on measuring Intrauterine adhesion, crosslinked hyaluronan gel, hysteroscopy, clinical trial

Eligibility Criteria

20 Years - 40 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Female patients who are 20-40 years old who is diagnosed as intrauterine adhesion, and did not receive adhesiolysis surgery.
  • Patients who signed the informed consent form (ICF) and agreed to take contraceptive measures within 3 months after the surgery.
  • Physical examination and routine laboratory tests demonstrated no systemic diseases.
  • According to the AFS scoring system on the IUA (1988) only those patients with moderate to severe IUA (i.e. total AFS score larger than 4 points) were enrolled in this clinical trial.

Exclusion Criteria:

  • Patients who is allergic to hyaluronan or its derivatives.
  • Patients with inflammation of reproductive organs, pelvic cavity inflammation, malignant tumor of reproductive organs and other systemic diseases that could cause metrorrhagia.
  • Patients with malformation of reproductive organs.
  • Patients who may not take effective contraceptive measures within 3 months after the surgery. Patients who were suffering severe systemic diseases such as coagulative disorders, cardiovascular diseases and long-term alcoholism and drug abuse were also excluded from this clinical trial.

Sites / Locations

  • The Third Xiangya Hospital of Central South University
  • The People's Hospital of Hunan Province
  • The People's Hospital of Chenzhou City,

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Treatment

Control

Arm Description

After the hysteroscopic adhesiolysis, crosslinked hyaluronic acid gel is applied into the uterine cavity, then a Foleys balloon catheter is inserted into the uterine cavity.

After hysteroscopic adhesiolysis, a Foleys balloon catheter is inserted into the unterine cavity.

Outcomes

Primary Outcome Measures

the percentage of patients free from IUA
Second look hysteroscopic examinations were performed at 3 months postoperatively. The adhesion was scored at adhesiolysis surgery and at follow-up hysteroscopy according to American Fertility Society scoring system.

Secondary Outcome Measures

Effective rate
Total AFS score
The score for each subcategory of AFS scoring system
The safety
Evaluated based on the number of patients shown complications and incidence rate for severe adverse events

Full Information

First Posted
August 18, 2014
Last Updated
August 18, 2014
Sponsor
Xiaozheng Shu
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1. Study Identification

Unique Protocol Identification Number
NCT02220621
Brief Title
Efficacy and Safety of Crosslinked Hyaluronan Gel for Preventing Intrauterine Adhesion
Official Title
A Prospective, Multi-center, Randomized, Controlled Clinical Study on Self-crosslinked Sodium Hyaluronate Gel for Prevention of Intrauterine Adhesion
Study Type
Interventional

2. Study Status

Record Verification Date
August 2014
Overall Recruitment Status
Completed
Study Start Date
October 2011 (undefined)
Primary Completion Date
April 2012 (Actual)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Xiaozheng Shu

4. Oversight

5. Study Description

Brief Summary
Intrauterine adhesion (IUA) is the adhesion of intrauterine tissues due to the exposure of myometrial tissues caused by the endometrial basal injury. IUA is clinically manifested as symptoms such as abdominal pain, hypomenorrhea or amenorrhea, sterility and habitual abortion, which seriously affect the patients quality of life. Preventing IUA has been tried using different methods such as barrier or stent in order to separate the opposing endometrium during the tissue healing processes. Although some successes have been reported there are still some challenges need to be dealt with. One of the barrier materials for preventing IUA is made of hyaluronic acid (HA). HA is a natural ECM of human tissue with excellent biocompatibility and promotes the scar-free wound repair. The self-crosslinked esterified HA gel has demonstrated the capacity to prevent IUA in clinical studies. A novel self-crosslinked HA gel is developed by BioRegen Biomedical(Changzhou)Co., Ltd with proprietary technologies. This product is a highly viscoelastic crosslinked gel that overcomes the shortcoming of sodium hyaluronate with high motility and too quick degradation in vivo. For this product, the results of animal experiments and various safety features have been designed and tested conforming to the national regulations and standards. In order to launch this product to the market, this prospective, randomized and controlled clinical trial is designed and will be performed to verify its safety/efficacy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Intrauterine Adhesion
Keywords
Intrauterine adhesion, crosslinked hyaluronan gel, hysteroscopy, clinical trial

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
120 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Treatment
Arm Type
Experimental
Arm Description
After the hysteroscopic adhesiolysis, crosslinked hyaluronic acid gel is applied into the uterine cavity, then a Foleys balloon catheter is inserted into the uterine cavity.
Arm Title
Control
Arm Type
Active Comparator
Arm Description
After hysteroscopic adhesiolysis, a Foleys balloon catheter is inserted into the unterine cavity.
Intervention Type
Device
Intervention Name(s)
Crosslinked hyaluronic acid gel
Other Intervention Name(s)
MateRegen Gel IU.
Intervention Description
After hysteroscopic adhesiolysis, MateRegen Gel IU is applied into the uterine cavity together with a Foley balloon catheter.
Intervention Type
Device
Intervention Name(s)
Foleys balloon catheter
Intervention Description
After adhesivolysis, the Foleys balloon catheter is inserted into the uterine cavityand expanded with normal saline.
Primary Outcome Measure Information:
Title
the percentage of patients free from IUA
Description
Second look hysteroscopic examinations were performed at 3 months postoperatively. The adhesion was scored at adhesiolysis surgery and at follow-up hysteroscopy according to American Fertility Society scoring system.
Time Frame
3 months after surgery
Secondary Outcome Measure Information:
Title
Effective rate
Time Frame
three months after surgery
Title
Total AFS score
Time Frame
3 months
Title
The score for each subcategory of AFS scoring system
Time Frame
3 months
Title
The safety
Description
Evaluated based on the number of patients shown complications and incidence rate for severe adverse events
Time Frame
3 months
Other Pre-specified Outcome Measures:
Title
Safety
Description
Severe adverse event (SAE): cause prolonged hospitalization and disability to the patient.
Time Frame
3 months

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Female patients who are 20-40 years old who is diagnosed as intrauterine adhesion, and did not receive adhesiolysis surgery. Patients who signed the informed consent form (ICF) and agreed to take contraceptive measures within 3 months after the surgery. Physical examination and routine laboratory tests demonstrated no systemic diseases. According to the AFS scoring system on the IUA (1988) only those patients with moderate to severe IUA (i.e. total AFS score larger than 4 points) were enrolled in this clinical trial. Exclusion Criteria: Patients who is allergic to hyaluronan or its derivatives. Patients with inflammation of reproductive organs, pelvic cavity inflammation, malignant tumor of reproductive organs and other systemic diseases that could cause metrorrhagia. Patients with malformation of reproductive organs. Patients who may not take effective contraceptive measures within 3 months after the surgery. Patients who were suffering severe systemic diseases such as coagulative disorders, cardiovascular diseases and long-term alcoholism and drug abuse were also excluded from this clinical trial.
Facility Information:
Facility Name
The Third Xiangya Hospital of Central South University
City
Changsha
State/Province
Hunan
ZIP/Postal Code
410013
Country
China
Facility Name
The People's Hospital of Hunan Province
City
Changshu
State/Province
Hunan
ZIP/Postal Code
410005
Country
China
Facility Name
The People's Hospital of Chenzhou City,
City
Chenzhou
State/Province
Hunan
ZIP/Postal Code
423000
Country
China

12. IPD Sharing Statement

Citations:
PubMed Identifier
12923149
Citation
Acunzo G, Guida M, Pellicano M, Tommaselli GA, Di Spiezio Sardo A, Bifulco G, Cirillo D, Taylor A, Nappi C. Effectiveness of auto-cross-linked hyaluronic acid gel in the prevention of intrauterine adhesions after hysteroscopic adhesiolysis: a prospective, randomized, controlled study. Hum Reprod. 2003 Sep;18(9):1918-21. doi: 10.1093/humrep/deg368.
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Efficacy and Safety of Crosslinked Hyaluronan Gel for Preventing Intrauterine Adhesion

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