Tolerance and Efficiency of Paracetamol Subcutaneous Injection

NCT02884609 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 160

Last updated 2019-04-16

No results posted yet for this study

Summary

The purpose of this study is to evaluate the tolerance and the efficiency of subcutaneous administration of Paracetamol for patients in palliative care.

Conditions

Sponsors & Collaborators

  • Centre Hospitalier Régional Metz-Thionville

    lead OTHER

Principal Investigators

  • Benoît LEHEUP, MD · CHR Metz-Thionville

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-08-31
Primary Completion
2018-07-31
Completion
2018-07-31

Countries

  • France

Study Locations

More Related Trials

Entities

Diseases

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 NCT02884609 on ClinicalTrials.gov