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Clinical Trials/NCT04300660
NCT04300660
Unknown
Not Applicable

POPARTS Study- Post-Operative Pain After Recovery in Thoracic Surgery: Evaluation of the Persistence of Painful Symptoms and the Incidence of Neuropathic Pain After Resective Lung Surgery

University of Trieste1 site in 1 country250 target enrollmentOctober 25, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Neuropathic Pain
Sponsor
University of Trieste
Enrollment
250
Locations
1
Primary Endpoint
Incidence of persistent post-operative pain after thoracic surgery
Last Updated
6 years ago

Overview

Brief Summary

Persistent pain after surgery has significant physical and mental consequences for the patient, as well as a significant economic impact on health systems. Neuropathic pain is caused by direct or indirect damage to the somatosensitive system. In thoracic surgery, chronic neuropathic pain is represented by Post-Thoracotomic Pain Syndrome (PTPS), defined as recurrent or persistent pain in the thoracotomy scar site that persists for more than 3-6 months. Currently, in literature, the prevalence of PTPS is extremely variable. This prospective observational study aims to assess the incidence of pain in the weeks and months following surgery and to assess whether and how the presence of painful symptoms changes the patient's quality of life.

Detailed Description

For each patient enrolled in the study, in the pre-operative phase, comorbidities, any chronic analgesic therapy and quality of life (through a dedicated questionnaire - Euro QoL 5D5L1) will be recorded. Surgical data (type of procedure, lobe affected by resection, type of approach and surgical time) and anesthesiological data (intravenous opioid, locoregional technique (s), non-opioid analgesics administered and other medications) will be collected in the perioperative phase. In the 48 hours following the surgery (in the Recovery Room, at 6h, 12h, 24h, 36h and 48h) the patient's pain data will be recorded (static, dynamic and cough-associated NRS) and those relating to any complications. The total amount of morphine administered to the patient in the first 48 hours will also be recorded. Each patient will be evaluated 7 days, 1, 3 and 6 months after the surgery by telephone interview. In this last phase, the possible presence of pain and its characteristics will be assessed, especially if these meet the criteria of neuropathic pain.

Registry
clinicaltrials.gov
Start Date
October 25, 2017
End Date
April 2020
Last Updated
6 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Marzia Umari

Principal Investigator

University of Trieste

Eligibility Criteria

Inclusion Criteria

  • Age ≥ 18 years
  • Patient's consent to the trial
  • Candidate to resective lung surgery (lobectomy, segmentectomy, atypical resection) with minimally invasive approach (mini-thoracotomy with muscle sparing or video-assisted thoracic surgery, VATS)

Exclusion Criteria

  • neurological and / or cognitive deficits
  • inability to obtain informed consent
  • surgeries that include wall resections (pleural, muscle, rib or nerve)
  • pneumonectomy
  • Previous thoracic surgery at the time of enrollment

Outcomes

Primary Outcomes

Incidence of persistent post-operative pain after thoracic surgery

Time Frame: the data needed to analyze the incidence and characteristics of pain will be collected at 1 month after surgery

The incidence of static, dynamic and cough-associated pain is assessed through the numerical rate scale (NRS), by a telephone interview one week and one month after surgery. A questionnaire is submitted to the patient to analyze the characteristics of the pain and its possible impact on the patient's quality of life.

Incidence of Chronic Pain after thoracic surgery

Time Frame: The data needed to analyze the presence of chronic pain will be collected at 6 months after surgery

The possible presence and incidence of chronic pain is assessed through a telephone interview three and six months after surgery.

Presence of pain with typical features of neuropathic pain in the different phases of the postoperative course

Time Frame: The data neede to analyze the presence of neuropathic pain will be collected at 6 months after the surgery

During each telephone interview the presence of neuropathic pain is assessed through a dedicated questionnaire (PainDetect Questionnaire) and the impact that this type of pain has on the patient's quality of life.

Secondary Outcomes

  • Assessment of the incidence of chronic pain based on the different surgical techniques in thoracic surgery(during the intraoperative phase, data relating to the surgical techniques performed are collected)
  • Assessment of the post-operative quality of life based on the different surgical techniques in thoracic surgery(during the intraoperative phase, data relating to the surgical techniques performed are collected)
  • Evaluation of postoperative pain control based on different anesthesiological techniques and its possible correlation with the development of chronic pain(data relating to this objective are collected in the intraoperative, 24 hours after surgery and subsequent telephone interviews at 1 week, 1, 3 and 6 months after thoracic surgery)

Study Sites (1)

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