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NCT05591521Completed

Evaluation of Pain in the Course of in Vitro Fertilization: the Endalgofiv-2 Study

Source: ClinicalTrials.gov · Last updated 26 Dec 2025

Brief summary (registry, in English)

The ENDALGOFIV study of pain assessment during the IVF pathway at Lille University Hospital, conducted from November 2018 to July 2020, showed that endometriosis patients have intense pain, particularly of a neuropathic nature, even before starting their IVF pathway compared to patients without endometriosis, but without an increase in pain scores during the IVF pathway. As a result of this study, a new pain management protocol for all patients undergoing IVF have been implemented in our MPA center. The study will be evaluated the impact of this new management. Main objective To evaluate the effect of the change in pain management protocol in all patients (endometriotic or not) undergoing IVF treatment during the study period by comparing them to the data of the ENDALGOFIV 1 study.

Status (registry)
Completed
Study type
Observational
Enrollment
206 (actual)
First submitted
11 Aug 2022
Start date
30 Nov 2022
Primary completion date
24 Mar 2024
Lead sponsor
University Hospital, Lille
NCT number
NCT05591521

What you commit to

  • Study type: Observational
  • Participants enrolled: 206
  • From 30 Nov 2022 to the primary completion date, 24 Mar 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Previously enrolled patient (ENDALGOFIV or ENDALGOFIV 2)

Age

  • Patient over 43 years old

Other

  • Refusal to participate in the study
  • Minor patient
  • BMI patient \> 35
  • Pregnant woman
  • Unable to provide clear information to the patient
  • Patient under guardianship or lack of health cover
  • Patient in IVF with donation of oocyte
  • IVF patients for oocyte preservation
  • Patient who had already participated in the study

Who the study is looking for

  • All patients who start an IVF cycle in the medically assisted procreation department of the Jeanne de Flandres Hospital (CHRU Lille)

Age in the registry: 18 years to 43 years · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Hop Jeanne de Flandre Chu Lille
Coordinator of this site? Confirm its status
LilleFranceUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.