Skip to content

Chest Kinesio Taping for pain control after lung lobectomy

Chest Kinesio Taping® for pain control after lobectomy for lung cancer: a randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN37253470
Enrollment
160
Registered
2015-12-10
Start date
2013-03-01
Completion date
Unknown
Last updated
2016-10-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postoperative chest pain after lung lobectomy Signs and Symptoms

Interventions

Standard postoperative analgesia are administered in both groups (paracetamol/NSAID, epidural analgesia including opioids), with supplemental analgesia i.v. boluses at patient request. On postoperativ

Sponsors

University of Insubria (Italy)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients undergoing lung lobectomy

Exclusion criteria

Exclusion criteria: 1. Age >85 2. Refusal 3. Previous exposure to Kinesio Taping 4. Recent trauma 5. Pre-existing pain or prolonged ICU treatment

Design outcomes

Primary

MeasureTime frame
Thoracic pain severity score [visual analog scale (VAS) ranging 0–10] is self-assessed by all patients on postoperative day 1, 2, 5, 8, 9 and 30

Secondary

MeasureTime frame
1. Request for supplemental analgesia; method used to measure: categorical variable: yes if any supplemental analgesic (non-steroidal anti-inflammatory drugs (NSAID) and/or opioids) are administered at patient request, more than standard postoperative analgesia during the postoperative period (from day of surgery to the day of discharge from hospital); no if no supplemental analgesics are requested by the patient nor administered more than standard analgesia during the in-hospital postoperative period; timepoint: day of discharge from the hospital 2. Chest tube duration (days); timepoint: from day of surgery to the day of last chest tube removal 3. Morbidity; method used to measure: categorical variable: yes if any postoperative complication occurs during the postoperative period within 30 days from day of surgery; no if no postoperative complication occurs within 30 days from day of surgery; timepoint: 30th postoperative day from surgery 4. Post-operative length of stay (days); timepoint: from day of surgery to the day of discharge from hospital

Countries

Italy

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 1, 2026