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Postoperative Pain After Single Port, Two Ports and Three Ports VATS Lobectomy

NCT03228056 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 90

Last updated 2018-04-11

No results posted yet for this study

Summary

This single-center, prospective, randomized controlled trial was designed to assess and compare the postoperative pain after VATS lobectomy performed though one, two and three incisions. The primary outcome measure is pain intensity measured in VAS scale. The secondary outcome measure is cumulative morphine consumption up to 72 hours after surgery

Conditions

Interventions

DIAGNOSTIC_TEST

pain intensity measured in VAS scale

Pain intensity in 0-100 mm VAS scale is measured every 4 hours on standard ruler beginning from the end of the surgery.

Sponsors & Collaborators

  • Pulmonary Hospital Zakopane

    lead OTHER

Principal Investigators

  • Marcin Zieliński, PhD · Pulmonary Hospital, Zakopane, Poland

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
PARALLEL

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-06-01
Primary Completion
2018-12-31
Completion
2018-12-31

Countries

  • Poland

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 NCT03228056 on ClinicalTrials.gov