A Prospective Multicenter Observational Real-world Study of Retained Products of Conception

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18-45
SponsorThe Third Xiangya Hospital of Central South University

About this trial

The purpose of this study is to explore the optimal treatment strategy for retained products of pregnancy. Compared with surgical treatment, prospectively observe whether drug-assisted expectant management until the right time for surgery reduce the occurrence of intrauterine adhesions, and thus protect fertility.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

None

Disqualifiers

None

Trial population

From June 2022 to June 2024, patients diagnosed with retained products of conception by ultrasound in the outpatient department.

Trial design

Design model

Case-control

Time perspective

Prospective

Treatments tested in this trial

  • Uterine curettage

    Procedure/Surgery

    Use intravenous general anesthesia (which can be assisted by laryngeal mask) (local anesthesia, epidural anesthesia or endotracheal intubation anesthesia can be selected in special cases), the patient takes the lithotomy position, the anesthesia effect is satisfactory, and the uterine distension fluid is normal saline. The uterine distension pressure is adjusted to maintain at 100-120 mmHg. It is recommended to use a diagnostic and therapeutic integrated hysteroscope with an outer diameter of \<5 mm (it is necessary to record the specific type of hysteroscope and instrument used) to enter the uterine cavity through the cervix to clarify the situation in the uterine cavity. Then explore the depth of the uterus. (Under ultrasonic monitoring) The cervical dilator sequentially dilates the cervix to 8-10 (depending on the outer diameter of the therapeutic hysteroscope used, hysteroscopic electroresection is not recommended), and select a 7mm outer diameter hysteroscope with a 3mm diameter.

  • Expectant care

    Drug

    Patients with no contraindications to medication should take 2mg Bid of Progynova (or a similar dose of Estoril) orally until after surgery (generally, Progynova is still used for about 2-4 weeks after surgery and progesterone withdrawal bleeding is used); take Yimucao granules or Wujia Biochemical Capsules orally for 2 weeks and then stop taking the medicine; check blood β-HCG every week; check uterine and bilateral adnexa 4D color Doppler ultrasound every 2-3 weeks; until the preset surgery time is reached: 1) blood β-HCG \<50mmol/L; 2) B-ultrasound measurement of the length from the internal cervical os to the uterine fundus ≤6cm; 3) the time interval from the previous surgery is at least 4 weeks; 4) Color Doppler ultrasound indicates that the blood flow level of the pregnancy and the attachment is 1-3.

Treatment groups

600 Participants
are divided into 2 treatment groups
Group A: Control group1 intervention
Group B: Experimental group1 intervention

Trial outcomes

Primary outcomes

1

Number of Participants with Intrauterine Adhesions (IUA) at 3 Months Post-Treatment

Intrauterine adhesions are diagnosed by three-dimensional transvaginal ultrasound or hysteroscopy. Adhesions are graded according to the American Fertility Society (AFS) classification. This outcome measures the incidence of IUA following different management strategies for retained products of conception, reflecting the degree of endometrial injury.

Time frame
At 3 months after completion of treatment (on the 16th-24th day of the third menstrual cycle post-treatment)
2

Number of Participants Requiring Secondary Surgical Evacuation

Secondary surgical evacuation is defined as any additional surgical procedure (hysteroscopic or curettage) required for complete removal of retained products of conception after the initial management strategy. This outcome reflects the effectiveness of the initial treatment approach and the number of intrauterine procedures.

Time frame
From initiation of treatment to 3 months post-treatment
3

Number of Participants Achieving Pregnancy within 1 Year after Attempting Conception

Pregnancy is defined as a positive serum β-hCG test and confirmed intrauterine gestational sac by ultrasound. This outcome is assessed only in participants with fertility intent and reflects the ultimate goal of fertility preservation.

Time frame
From the start of attempting pregnancy (after completion of treatment and at least one normal menstrual cycle) up to 1 year

Secondary outcomes

1

Number of Participants with Active Bleeding During Expectant Management

Active bleeding is defined as vaginal bleeding exceeding twice the normal menstrual volume, requiring emergency hospitalization or surgical intervention during the expectant management period. This outcome reflects the safety of expectant management.

Time frame
From enrollment to hospitalization or intervention, assessed up to 3 months
2

Number of Participants with Pelvic Infection During Expectant Management

Pelvic infection is defined as the presence of clinical signs (fever, pelvic pain, purulent discharge) and/or laboratory evidence (elevated white blood cell count, CRP, procalcitonin) requiring antibiotic therapy or surgical intervention. This outcome reflects the safety of expectant management.

Time frame
From enrollment to hospitalization or intervention, assessed up to 3 months
3

Number of Participants with Live Birth Following Subsequent Pregnancy

Live birth is defined as the delivery of any viable infant (≥24 weeks of gestation). This outcome is the most definitive measure of reproductive outcome following treatment.

Time frame
At delivery, assessed up to 1 year after pregnancy confirmation
4

Intraoperative Blood Loss During Hysteroscopic Surgery

Estimated blood loss (in mL) during hysteroscopic removal of retained products of conception. This outcome reflects surgical complexity and the invasiveness of the procedure.

Time frame
During the surgical procedure

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

The Third Xiangya Hospital of Central South University

Lead sponsor

Changsha Hospital for Maternal and Child Health Care

Collaborator

ZhuZhou Central Hospital

Collaborator

Xiangtan Central Hospital

Collaborator

Xiangtan Hospital for Maternal and Child Health Care

Collaborator

Yiyang Hospital for Maternal and Child Health Care

Collaborator

The First People's Hospital of YueYang

Collaborator

The First People's Hospital of Changde City

Collaborator

The First Affiliated Hospital of Shaoyang University

Collaborator

Hunan University of Medicine General Hospital

Collaborator

Hengyang Central Hospital

Collaborator

Chenzhou Hospital for Maternal and Child Health Care

Collaborator

Yongzhou Center Hospital

Collaborator

Hunan Provincial People's Hospital

Collaborator

Changsha Maternal and Child Health Hospital

Collaborator

Liuyang People's Hospital

Collaborator