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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04936347
Other study ID # Z191100006619058
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date August 1, 2019
Est. completion date August 31, 2022

Study information

Verified date June 2021
Source Fu Xing Hospital, Capital Medical University
Contact Xiaowu Huang
Phone +8613810828816
Email hxiaowu_fxyy@126.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In this prospective, randomized controlled trial,the investigators wish to explore the difference of therapeutic effect and prognosis between "hot knife" and "cold knife" in the treatment of uterine adhesion under hysteroscopy.


Description:

1. Study Design:This is a prospective, randomized controlled trial.The investigators use hysteroscopy finding as standard reference. 2. Study population 802 patients diagnosed with intrauterine adhesions(IUA)will be prospectively recruited. Before the surgery all patients will undergo preoperative evaluations, including a detailed history of the menstrual pattern,any previous intrauterine surgery, and reproductive history, as well as trans-vaginal ultrasonography.The severity and extent of intrauterine adhesions will be scored according to the ESGE IUA grades. 3. Randomization: Randomization was performed electronically using SPSS statistical software version 26.0 (SPSS, Inc., Chicago, IL,USA) by the investigator.802 recruited patients will be randomized to one of the two treatment groups by computer-generated numbers: the control group("hot knife" group) and the experimental group("cold knife" group). 4. Surgical technique: - Hysteroscopic surgery will be performed in a standardized manner.The procedure will be performed under general anesthesia. Ultrasonographic guidance will be routinely used. - The interference of "cold knife" group (the experimental group) including 401 IUA patients is to perform intrauterine adhesiolysis with scissors, while the interference of "hot knife" group (the control group) is to perform intrauterine adhesiolysis with bipolar electric needle electrode, part of the scar tissue removed by electronic loop when it is necessary. - A Foley-catheter filled with 3.0-5.0 ml normal saline will be inserted into the uterus for 5-7 days after surgery. 5. Postoperative treatments - All subjects will be treated with oral antibiotics for 5-7 days. - All subjects will be treated with Hormone therapy. - A second-look hysteroscopy will be carried out in the early proliferative phase 4 weeks after the surgery and an optional third-look hysteroscopy will be carried out 8 weeks after the surgery. 6. Follow up: - Follow-up styles: the doctor's outpatient review, telephone, WeChat and so on. - Follow-up time:1 month, 2months, 12 months after the operation. - Follow up the results of hysteroscopy and the menstrual improvement and pregnancy outcomes at 12 months after the operation. 7. Consent: All subjects will be given a detailed explanation of the study and sufficient time to consider their participation. A written consent form will be signed by the patient and retained in the records.


Recruitment information / eligibility

Status Recruiting
Enrollment 802
Est. completion date August 31, 2022
Est. primary completion date December 31, 2021
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria: - Indications: fertility desire, periodic pelvic pain; - Women aged 18-40 years; - Moderate to severe intrauterine adhesion(ESGE Grade II-IV); - All enrolled women provided written informed consent and agree to the entire study protocol prior to surgery Exclusion Criteria: - Contraindications: such as severe medical diseases, pregnancy status, reproductive tract infection, malignant tumor; - History of uterine artery embolization; - Infertility caused by male factors or ovarian dysfunction or premature ovarian failure

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
cold knife
Transcervical resection of adhesions is performed with scissors to restore the shape of uterine cavity, promote the regeneration and repair of endometrium, and ultimately improve the reproductive prognosis of patients.
hot knife
Transcervical resection of adhesions is performed with bipolar electric cutting to restore the shape of uterine cavity, promote the regeneration and repair of endometrium, and ultimately improve the reproductive prognosis of patients.

Locations

Country Name City State
China Fu Xing Hospital, Capital Medical University Beijing

Sponsors (1)

Lead Sponsor Collaborator
Fu Xing Hospital, Capital Medical University

Country where clinical trial is conducted

China, 

References & Publications (6)

AAGL Elevating Gynecologic Surgery. AAGL practice report: practice guidelines on intrauterine adhesions developed in collaboration with the European Society of Gynaecological Endoscopy (ESGE). Gynecol Surg. 2017;14(1):6. doi: 10.1186/s10397-017-1007-3. Epub 2017 May 1. — View Citation

Guo EJ, Chung JPW, Poon LCY, Li TC. Reproductive outcomes after surgical treatment of asherman syndrome: A systematic review. Best Pract Res Clin Obstet Gynaecol. 2019 Aug;59:98-114. doi: 10.1016/j.bpobgyn.2018.12.009. Epub 2019 Jan 3. — View Citation

Hooker AB, Lemmers M, Thurkow AL, Heymans MW, Opmeer BC, Brölmann HA, Mol BW, Huirne JA. Systematic review and meta-analysis of intrauterine adhesions after miscarriage: prevalence, risk factors and long-term reproductive outcome. Hum Reprod Update. 2014 — View Citation

Khan Z, Goldberg JM. Hysteroscopic Management of Asherman's Syndrome. J Minim Invasive Gynecol. 2018 Feb;25(2):218-228. doi: 10.1016/j.jmig.2017.09.020. Epub 2017 Oct 9. Review. — View Citation

Valle RF, Sciarra JJ. Intrauterine adhesions: hysteroscopic diagnosis, classification, treatment, and reproductive outcome. Am J Obstet Gynecol. 1988 Jun;158(6 Pt 1):1459-70. — View Citation

Yu D, Wong YM, Cheong Y, Xia E, Li TC. Asherman syndrome--one century later. Fertil Steril. 2008 Apr;89(4):759-79. doi: 10.1016/j.fertnstert.2008.02.096. Review. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Recurrence rate Recurrence rate of intrauterine adhesions 2 months after surgery
Secondary Pregnancy rate The conception rate 1 year after the patient desire for pregnancy
Secondary Menstrual improvement rate The patients' estrual improvement rate 2 months after surgery
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