Treatment outcomes after cesarean scar pregnancy surgeries

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This prospective study compares various surgical approaches to remove cesarean scar pregnancy and repair the uterine scar, aiming to understand how each method influences treatment success and subsequent pregnancy results. Procedures include excisional surgeries via transvaginal excision or hysteroscopy-assisted laparoscopy, with conservative methods like ultrasound-guided vacuum aspiration for tissue removal. Participants are adult women with a prior cesarean delivery and a confirmed cesarean scar pregnancy, without major comorbidities, who can safely undergo surgery. The study is conducted at Zhejiang University’s Women’s Hospital and is led by that institution. Outcomes of interest include immediate treatment results and future pregnancy outcomes, with no control group specified in the provided details.

Why it matters

Who can join: the full rules

Inclusion Criteria:

1. Women over 18 years old with a history of cesarean section
2. Ultrasound diagnosis of cesarean scar pregnancy
3. No severe internal or external diseases, such as liver disease, kidney disease, cardiovascular disease, cerebrovascular disease, etc., and able to tolerate surgery

Exclusion Criteria:

1. Women under the age of 18
2. CSP patients who have received treatment in other hospitals

Where it's running

• Women's Hospital School Of Medicine Zhejiang University
  Hangzhou, Zhejiang, China Recruiting

Study contacts

• Principal investigator: xiuxiu jiang — women's hospital school of medicine Zhejiang uni
• Study coordinator: xiuxiu jiang, ph.D
• Email: jaingxiuxiu0418@zju.edu.cn
• Phone: 0086-571-87061501

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

• Surgical removal versus ultrasound-guided evacuation for cesarean scar pregnancy

  This will test whether surgical removal or ultrasound-guided evacuation works better and safer for people with type II cesarean scar pregnancy in the first trimester.

  Recruiting Sohag University · Sohag · NCT07166627

• Impact of bladder flap on cesarean scar niche after first cesarean

  This study tests whether omitting or keeping a bladder flap during a first cesarean affects the development of a cesarean scar niche seen about 6–8 weeks after delivery.

  Recruiting at 2 sites Montefiore Medical Center · The Bronx, New York and 1 other locations · NCT07634679

• Impact of Barbed Suture on Uterine Healing After Cesarean Section

  This study tests if using barbed sutures instead of regular sutures during cesarean sections helps pregnant women heal better and reduces complications.

  Recruiting Hospital Clinic of Barcelona · Barcelona · NCT06691750

• Single-layer versus double-layer uterine closure after cesarean and myometrial thickness

  This trial tests whether closing the uterus with one layer or two layers during cesarean leads to thicker, healthier scar tissue in women having a cesarean delivery.

  Recruiting Ankara City Hospital Bilkent · Ankara, Not Valid · NCT07323355

• Amniotic membrane and calcium alginate dressing to help cesarean wounds heal

  This trial will test whether a biodegradable dressing made from amniotic membrane and calcium alginate helps women having elective cesarean sections heal their surgical wound faster and form a better scar.

  Recruiting Asfendiyarov Kazakh National Medical University · Almaty · NCT07241013

• Closing the uterus during cesarean: include or exclude the decidual layer to see if the scar heals better

  This randomized trial tests whether including or sparing the decidual layer when closing the uterus at cesarean delivery leads to better scar healing 6 to 9 months later for first-time mothers.

  Recruiting Kantonsspital Baden · Baden, Canton of Aargau · NCT07608874

How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.