Skip to content

Investigating immediate pain and post surgical recovery following laparoscopic surgery for diagnosis or treatment of endometriosis

Investigating immediate pain and post surgical recovery following laparoscopic surgery for diagnosis or treatment of endometriosis: a prospective cohort study.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ANZCTR
Registry ID
ACTRN12620001368921
Acronym
N/A
Enrollment
209
Registered
2020-12-18
Start date
2021-06-02
Completion date
2023-12-21
Last updated
2024-09-02

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

Conditions

None listed

Brief summary

Endometriosis is a common yet under-recognised chronic disease. Endometriosis occurs when cells similar to those that line a persons uterus grow in other parts of their body, usually around the pelvis. Although endometriosis is often effectively managed, it can lead to debilitating chronic and persistent pelvic pain and compromised fertility. It can also significantly impact the social and economic participation and psychosocial health of those affected. it is estimated that 11.4% (more than 830 000) Australian people are living with endometriosis; however, delays in diagnosis and lack of definitive research on the domestic burden of disease suggest the number could be far higher. Surgery for endometriosis is a common procedure and randomised, placebo controlled trials have shown a benefit at 6 and 12 months following surgery, with variable changes noted in these studies in the first few months. People with endometriosis frequently report a worsening of pain following their surgery, however there are no data reporting immediate outcomes, effect on menstruation or the likely changes to expect in these first few months. Our aim is to investigate the immediate effect of surgery on people's symptoms and provide that information in publicly available forums to improve the education and understanding of how women experience symptoms in the immediate post-operative phase of care. It is important to note that we are not establishing the long-term outcomes since these are reported in other studies.

Interventions

Patients who present to our hospital and clinics and across Australia with endometriosis-associated symptoms (e.g. dysmenorrhoea, non-menstrual pelvic pain, dyspareunia, dyschezia, dysuria, subfertility etc.) undergoing a planned laparoscopy to diagnose and/or treat endometriosis will be followed up for three months post laparoscopy. Data will be collected using the National Endometriosis Clinical and Scientific Trials (NECST) Network database.

Sponsors

Royal Hospital for Women
Lead SponsorHospital

Eligibility

Sex/Gender
All
Age
18 Years to 45 Years
Healthy volunteers
No

Inclusion criteria

- People with endometriosis. This may be women, people who identify as non-binary, or transgender men. - Participants being investigated for their endometriosis-related symptoms undergoing a planned surgical procedure. - Participants fluent in spoken and written English - Willingness to give written informed consent and willingness to participate to and comply with the study

Exclusion criteria

- Patients lactating, pregnant or of childbearing potential who are not willing to avoid becoming pregnant during the study - Patient known or suspected to have a malignancy - Patients who may become distressed because of their involvement in the study

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026