MedTrace Logo

Identification of Clinical, Biometrical and Operatory Factors Related to Pain During Cataract Surgery

NCT04353843 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 400

Last updated 2020-06-05

No results posted yet for this study

Summary

Adults who undergo cataract surgery will be questioned after surgery about the eventual pain they experienced, about their health history, personal treatment. If they accept to be included in the study we'll record different parameters related to the surgery: type of anesthesia, duration of surgery, machines used, unexpected events, particularities noticed by the surgeon, etc.

There will be no unusual intervention, everything will be run exactly as if there was no study. No additional consultation needed.

Conditions

  • Cataract

Sponsors & Collaborators

  • Centre Hospitalier Universitaire de Nīmes

    collaborator OTHER

  • Beziers Champeau Clinic

    collaborator UNKNOWN

  • Montpellier Beau Soleil Clinic

    collaborator UNKNOWN

  • Montpellier Ophtalmology Center

    collaborator UNKNOWN

  • University Hospital, Montpellier

    lead OTHER

Principal Investigators

  • Vincent Daien, MD, PhD, HDR · University Hospitals of Montpellier

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-05-01
Primary Completion
2021-05-01
Completion
2021-05-30

Countries

  • France

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04353843 on ClinicalTrials.gov