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Procedural Pain in Palliative Care: Prevalence, Intensity and Treatment

A

Antea Foundation

Status

Completed

Conditions

Pain Due to Certain Specified Procedures
Terminal Disease
Breakthrough Pain
Cancer
Pain

Treatments

Procedure: Personal Hygiene Care
Procedure: Subcutaneous drugs administration
Procedure: Wound care
Procedure: Mobilization
Procedure: Bladder catheterization
Procedure: Positioning

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

This study aims to assess self reported procedural pain compared with background pain and evaluate pain intensity differences across six standard procedures. Besides, rescue and preventive treatments used to control procedural pain will be examined.

Enrollment

1,079 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients receiving the procedures included in this study as a part of their standard care
  • Patients that have expressed their consent to participate to the study by signing the informed consent document

Exclusion criteria

  • Very serious or unstable clinical conditions with a Karnofsky Performance Status Index (KPS) < 20
  • Presence of neurological or psychiatric conditions, due to the original disease or concomitant diseases, interfering with the patient's level of consciousness or with judgment, such as to compromise compliance with the study protocol;
  • Not adequately controlled background pain (average NRS in the last 24 hours is > 4)
  • Emergency procedures or procedures performed during night time (from 8 p.m. until 8 a.m)

Trial design

1,079 participants in 1 patient group

Patients receiving standard procedures
Treatment:
Procedure: Personal Hygiene Care
Procedure: Subcutaneous drugs administration
Procedure: Wound care
Procedure: Mobilization
Procedure: Positioning
Procedure: Bladder catheterization

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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