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Clinical Trials/NCT05677269
NCT05677269
Recruiting
Not Applicable

The (Cost-)Effectiveness of Surgical Excision of Colorectal Endometriosis Compared to ART Treatment Trajectory

Leiden University Medical Center10 sites in 1 country339 target enrollmentFebruary 17, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Endometriosis, Rectum
Sponsor
Leiden University Medical Center
Enrollment
339
Locations
10
Primary Endpoint
Cumulative live birth rate
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

To goal of this study is to determine whether laparoscopic resection of colorectal endometriosis results in an increased cumulative live birth rate (CLBR) both spontaneous and after ART (including in vitro fertilization (IVF) or intracytoplasmic sperm injection (ICSI), and better patient reported outcome measures (PROMs) compared to an IVF/ICSI treatment trajectory.

Detailed Description

Endometriosis is characterized by extra-uterine endometrium like tissue and affects 10-15% of the women in their reproductive years and in 5-12% of these women colorectal endometriosis is present. The quality of life is lowered due to severe pain symptoms (dysmenorrhea, dyschezia, dysuria, chronic pelvic pain) and subfertility.The management of colorectal endometriosis-related subfertility is challenging. While the impact of colorectal endometriosis per se remains inconclusive as other intraperitoneal endometriosis lesions are frequently present, fertility is most likely affected by multiple mechanisms including inflammatory alterations in peritoneal fluid, alterations in estrogen and progesterone hormone levels, lowered endometrium receptivity, associated adenomyosis, a lower ovarian reserve (in case endometriomas are present) and adhesion formation that disrupts adnexal anatomy and function. Usually, surgery is preferred in case of dominant pain complaints, while IVF/ICSI is started when the wish to conceive is dominant. Recent evidence suggests a CLBR of 44.9% in patients with rectosigmoid endometriosis treated by surgery compared to 55.9% after 4 cycles of IVF/ICSI treatment without surgery. In the Netherlands, the number of reimbursed IV/ICSI attempts in limited to three. In addition, a combined strategy may result in even higher cumulative live birth rates. However, the place and optimal timing of surgery in patients with colorectal endometriosis and a desire to have children is unknown. To provide robust evidence that can be extrapolated to the Dutch healthcare system, this study aims to determine whether surgical excision of colorectal endometriosis results in increased CLBR both spontaneous and after IVF/ICSI, and better PROMs compared to an IVF/ICSI treatment trajectory.

Registry
clinicaltrials.gov
Start Date
February 17, 2023
End Date
January 1, 2029
Last Updated
last year
Study Type
Observational
Sex
Female

Investigators

Sponsor
Leiden University Medical Center
Responsible Party
Principal Investigator
Principal Investigator

mdblikkendaal

Principle Investigator

Leiden University Medical Center

Eligibility Criteria

Inclusion Criteria

  • Colorectal endometriosis defined as endometriosis involving the (colo)rectum:
  • #Enzian classification score C1,C2,C3 (C=rectum) or FI (F=far locations, I=sigmoid colon) detected with ultrasound or MRI;
  • Women in a heterosexual or in a same-sex relationship;
  • The patient has an active wish to conceive and experiences at least one of the following criteria:
  • At least one year of non-conception (either spontaneous of after intra uterine inseminations)
  • Inability to have timed intercourse because of pain (dyspareunia and/or chronic pelvic pain)
  • Severe complaints (expectant management is not acceptable (anymore)
  • The patients has an indication for IVF/ICSI according to Dutch guidelines (Werkgroep netwerkrichtlijn, december 2010);
  • failed intra uterine insemination
  • male factor subfertility (oligoasthenoteratozoospermia defined as VCM \<1 million)

Exclusion Criteria

  • Patients with deep endometriosis without colorectal involvement;
  • Patients who conceive spontaneously prior to intervention;
  • Patients requiring surgery on short notice and therefore unable to opt for IVF/ICSI (e.g. in case of unilateral or bilateral hydronephrosis, severe bowel stenosis and suspicion of an impending ileus);
  • Patients with a contra-indication for IVF/ICSI (e.g. diminished ovarian reserve (premature ovarian failure) (AMH (when available) \<p10 adjusted for age), untreated congenital uterine abnormalities, maltreated/untreated systemic or malignant disease or severe risk factors for oocyte aspiration);
  • Patients diagnosed with other diseases causing infertility (e.g. recurrent miscarriages, antiphospholipid syndrome);
  • Not able to read and understand Dutch or English.

Outcomes

Primary Outcomes

Cumulative live birth rate

Time Frame: At the end of the study period (live birth or after 3 IVF/ICSI attempts and/or surgery in the follow-up period (40 months) )

Live birth is defined as the complete expulsion or extraction from a women of a product of fertilization, after 20 weeks of gestational age; which, after such separation, breathes or shows any other evidence of life, such as heart beat, umbilical cord pulsation or definite movement of voluntary muscles, irrespective of whether the umbilical cord has been cut of the placenta is attached. A birth weight of 350 grams or more can be used if gestational age is unknown

Secondary Outcomes

  • Bowel specific symptoms(At baseline (T=0: when informed consent is granted), 12, 24 and 36 months and in case of surgery, before surgery.)
  • Productivity costs(At baseline (T=6, 12, 18, 24, 30, 36 and 40 months and in case of surgery, before surgery.)
  • Complications(At the end of the study period (live birth or after 3 IVF/ICSI attempts and/or surgery in the follow-up period (40 months) ))
  • Quality of life in general(At baseline (T=0: when informed consent is granted), 6, 12, 18, 24, 30, 36 and 40 months and in case of surgery, before surgery.)
  • Pain scores(At baseline (T=0: when informed consent is granted), 12, 24 and 36 months and in case of surgery, before surgery.)
  • Medical costs per group(At the end of the study period (live birth or after 3 IVF/ICSI attempts and/or surgery in the follow-up period (40 months) ))
  • Endometriosis specific symptoms(At baseline (T=0: when informed consent is granted), 12, 24 and 36 months and in case of surgery, before surgery.)

Study Sites (10)

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