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The Impact of Surgical Treatment of Endometriomas on Ovarian Reserve

The Impact of Surgical Treatment of Ovarian Endometriomas on Ovarian Reserve: a Randomised Controlled Trial of Laparoscopic Ovarian Cystectomy Versus Cyst Ablation - a Pilot Study

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01425333
Enrollment
20
Registered
2011-08-30
Start date
2011-04-30
Completion date
2013-02-28
Last updated
2011-08-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Endometriosis

Keywords

Ovarian endometriomas, Laparoscopy, Cystectomy, Ablation

Brief summary

The aim of this study is to assess which of two commonly used surgical procedures in the treatment of ovarian cysts called endometriomas (cutting out of the cyst - cystectomy, or draining it and cauterising it's inner lining - ablation) causes the least damage to the ovary and is therefore best at maintaining the future fertility potential of a patient.

Interventions

PROCEDURESurgery for ovarian endometrioma

Patients undergoing surgery for ovarian endometrioma

Sponsors

University Hospitals of Derby and Burton NHS Foundation Trust
CollaboratorOTHER
Saad Amer
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 42 Years
Healthy volunteers
Yes

Inclusion criteria

* Women undergoing laparoscopic surgery for treatment of unilateral endometriomas measuring ≥ 3cm and ≤ 8cm in diameter

Exclusion criteria

* Patients who have received oestrogen suppressing drugs (e.g. oral contraceptive pills, GnRHa) during the previous six months * Patients who have previously undergone surgical treatment of endometriomas * Patients with bilateral endometriomas * Patients with endometriomas of less than 3cm in size or more than 8cm in size * Pre-surgical evidence of reduced ovarian reserve * Pregnant patients * Patients unable to give informed consent e.g. patients with mental incapacity

Design outcomes

Primary

MeasureTime frameDescription
Anti-Mullerian Hormone (AMH)6 months post-operativelyChange in anti-mullerian hormone level after surgery (at one week, three months and six months)

Secondary

MeasureTime frameDescription
Follicle Stimulating Hormone (FSH)6 monthsChange in follicle stimulating hormone levels after surgery (at one week, three months and six months)
Antral Follicle Count (AFC)3 monthsChange in AFC after surgery (at three months)

Countries

United Kingdom

Contacts

Primary ContactSaad Amer, MD, MRCOG
saad@amer@nottigham.ac.uk+44(1332)724612

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026