A Study of Women Receiving Standard of Care (SOC) for the Treatment of Pelvic Pain Due to Suspected or Confirmed Endometriosis and the Impact on the Disease or Symptom Progression.

A Multicenter, Observational Cohort Study of Women Receiving Standard of Care (SOC) for the Treatment of Pelvic Pain Attributable to Suspected or Confirmed Endometriosis

Status

Terminated

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT04140175

Enrollment

291

Registered

2019-10-25

Start date

2020-01-20

Completion date

2020-11-19

Last updated

2021-11-22

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

Conditions

Chronic Pelvic Pain, Dysmenorrhea, Endometriosis

Keywords

Endometriosis, Chronic Pelvic Pain, Dysmenorrhea

Brief summary

This study will describe historic, current, and evolving treatment pathways, treatments, and interventions in women with a suspected or confirmed diagnosis of endometriosis in order to better understand the impact of early intervention on the disease or its symptoms. Length of treatment is dependent on standard of care treatment provided and all study information will be collected during routine standard of care visits.

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

FEMALE

Age

12 Years to No maximum

Healthy volunteers

Inclusion criteria

* Women of reproductive age (between their first menstrual cycle and before onset of menopause). * Women who have experienced chronic pelvic pain (CPP) and/or dysmenorrhea (DYS) for at least 6 months prior to enrollment without symptom improvement with non-steroidal anti-inflammatory drugs (NSAIDs) or hormone/medical treatment. * Women with suspected or confirmed endometriosis (EM) at time of enrollment. * Women with CPP and/or DYS impacting daily activities as determined by their treating physician. * Able to read, understand and respond to patient questionnaires. * Willing to sign a patient authorization and/or informed consent form (ICF) and agree to disclose personal health information. NOTE: For pediatric patients, parental/guardian assent/ICF is also required.

Exclusion criteria

* Women with chronic pelvic pain (CPP) and/or dysmenorrhea(DYS) for reasons other than endometriosis (EM). * Women who have had a hysterectomy and/or bilateral ovary removal (oophorectomy). * Women who are pregnant or planning to become pregnant. * Women currently using assisted reproductive technologies such as in vitro fertilization (IVF). * Women with a history of, or current malignancy (with or without systemic chemotherapy) with the exception of basal cell carcinoma of the skin. * Women who are currently participating in an interventional clinical trial.

Design outcomes

Primary

Measure	Time frame	Description
Percentage of participants using specific medications for the treatment of chronic pelvic pain (CPP) and/or dysmenorrhea (DYS)	From onset of CPP and/or DYS to up to 4 years following study enrollment.	Data regarding medication use for CPP and/or DYS will be collected from participant medical records, health care provider questionnaires, and participant completed questionnaires.
Percentage of participants who underwent surgical interventions for the treatment of CPP and/or DYS	From onset of CPP and/or DYS to up to 4 years following study enrollment.	Percentage of participants who underwent surgical interventions for the treatment of CPP and/or DYS at any point from onset of CPP and/or DYS and study completion.
Number of surgical interventions for the treatment of CPP and/or DYS	From onset of CPP and/or DYS to up to 4 years following study enrollment.	Number of surgical interventions for the treatment of CPP and/or DYS.
Percentage of participants undergoing hysterectomy	From study enrollment (Week 0) to up to 4 years.	Percentage of participants undergoing hysterectomy during study enrollment.
Percentage of participants undergoing infertility treatment	From study enrollment (Week 0) to up to 4 years.	Percentage of participants undergoing infertility treatments during study enrollment.
Percentage of participants undergoing surgery	From study enrollment (Week 0) to up to 4 years.	Percentage of participants undergoing surgery as treatment for CPP and/or DYS.
Percentage of participants with complications associated with surgery	From study enrollment (Week 0) to up to 4 years.	Percentage of participants with complications associated with surgery.
Percentage of participants receiving specific treatment sequences for the treatment of CPP and/or DYS	From onset of CPP and/or DYS to up to 4 years following study enrollment.	Treatment sequences will be identified from the data. Treatment switching, add-on treatment, and discontinuations (including reasons) will be collected wherever possible.

Countries

United States

Outcome results