Assessment of Ovarian Reserve in the Treatment of Ovarian Endometrioma With Cystectomy or Argon Plasma Coagulation: A Aandomized Clinical Trial
1 other identifier
interventional
146
1 country
1
Brief Summary
Endometriosis is a benign, chronic, and often recurrent gynecological disease affecting approximately 10% of women of reproductive age. Among the different manifestations of the disease, ovarian endometrioma represents one of the most common forms, occurring in up to 50% of affected patients. Endometriomas may cause progressive damage to ovarian tissue through both mechanical effects and direct toxic effects related to the inflammatory and oxidative content of the cyst, ultimately leading to a reduction in ovarian reserve. When medical treatment is insufficient or not indicated, surgery represents a therapeutic option. The aim of surgery is to remove the cyst while minimizing the risk of recurrence and preserving as much healthy ovarian tissue as possible. Currently, the most widely used surgical technique is laparoscopic cystectomy performed by stripping the cyst capsule. However, this procedure may result in the inadvertent removal of healthy ovarian tissue and a consequent reduction in ovarian reserve. In recent years, ablative surgical techniques have been developed with the aim of reducing damage to the ovarian parenchyma. Among these, Argon Plasma Coagulation (APC) is a technique that uses a high-energy argon plasma jet to vaporize and coagulate superficial tissues. From a histological perspective, APC induces limited-depth tissue necrosis, generally confined to the cyst capsule, potentially reducing the risk of damage to the underlying ovarian tissue. In addition, this technology may offer practical and economic advantages. Several studies suggest that ablative techniques may have a lower impact on ovarian reserve compared with cystectomy, as assessed by antral follicle count and serum anti-Müllerian hormone (AMH) levels, a reliable biomarker of ovarian reserve. However, the available evidence mainly derives from observational studies or studies using ablative technologies different from the one investigated in the present study. Furthermore, the systematic use of ablative techniques remains controversial in clinical practice, partly because of the potential risk of recurrence associated with residual endometriotic tissue. To date, no randomized clinical trials have directly compared the impact of APC versus cystectomy on ovarian reserve in patients with ovarian endometrioma. Moreover, data are lacking regarding recurrence risk, post-treatment ovarian ultrasound characteristics following APC ablation, and the histological effects of this technique on endometriotic cysts. In light of these considerations, the present randomized clinical trial aims to compare the effect of cystectomy and Argon Plasma Coagulation ablation on the preservation of ovarian reserve in patients undergoing surgical treatment for ovarian endometrioma, while also evaluating ultrasound outcomes and recurrence risk during follow-up.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Jun 2026
Longer than P75 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
June 8, 2026
CompletedFirst Submitted
Initial submission to the registry
June 19, 2026
CompletedFirst Posted
Study publicly available on registry
June 24, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 8, 2028
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 8, 2029
June 24, 2026
June 1, 2026
2 years
June 19, 2026
June 19, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Late effects of APC or cystectomy on the AFC of the treated ovary
Change in antral follicle count (ΔAFC) of the treated ovary between baseline (T0) and 12 months (T2).
12 months after surgery (T2).
Secondary Outcomes (8)
Early effects of APC or cystectomy on the AFC of the treated ovary
40-60 days after surgery (T1).
Late effects of APC or cystectomy on serum AMH levels
12 months after surgery (T2).
Early effects of APC or cystectomy on serum AMH levels
40-60 days after surgery (T1).
Temporal pattern of AFC variation
Baseline (T0), 40-60 days after surgery (T1), 12 months after surgery (T2)
Temporal pattern of AMH variation
Baseline (T0), 40-60 days after surgery (T1), 12 months after surgery (T2)
- +3 more secondary outcomes
Study Arms (2)
Argon Plasma Coagulation (APC) ablation
EXPERIMENTALCyst opening and drainage, ablation of the inner surface of the cyst capsule using APC, and multiple biopsies of the cyst capsule.
Cystectomy
NO INTERVENTIONRemoval of the cyst capsule using the stripping technique, followed by ultra-selective hemostasis with bipolar energy and suturing of the ovarian parenchyma for hemostatic and reconstructive purposes (when indicated).
Interventions
Cyst opening and drainage, ablation of the inner surface of the cyst capsule using APC, and multiple biopsies of the cyst capsule.
Eligibility Criteria
You may qualify if:
- Symptomatic patients (pain and/or infertility) affected by ovarian endometriomas (unilateral or bilateral).
- Age between 18 and 40 years.
- Ultrasound diagnosis of one or more mono- or bilateral endometriotic cysts, with a maximum overall diameter (per ovary) ≤ 80 mm and at least one cyst diameter ≥ 20 mm.
- Use of hormonal therapy for at least 1 month prior to surgery.
- Willingness to undergo follow-up at 40-60 days and 12 months, according to clinical practice.
- Willingness to receive postoperative hormonal therapy, according to clinical practice, to minimize the risk of recurrence.
- Written informed consent obtained.
You may not qualify if:
- History of unilateral ovariectomy/adnexectomy or hysterectomy.
- Ultrasound evidence of other non-endometriotic ovarian cysts requiring surgical removal.
- Atypical endometrioma or ultrasound suspicion of malignancy.
- Previous surgery on one or both ovaries within 12 months prior to surgery.
- Known or suspected active oncological disease.
- Inability to undergo transvaginal ultrasound examination (patients with intact hymen).
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
IRCCS Azienda Ospedaliero-Universitaria di Bologna
Bologna, Bologna, 40138, Italy
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
June 19, 2026
First Posted
June 24, 2026
Study Start
June 8, 2026
Primary Completion (Estimated)
June 8, 2028
Study Completion (Estimated)
December 8, 2029
Last Updated
June 24, 2026
Record last verified: 2026-06