Pain Multidisciplinar Intervention in Major Trauma Patients

NCT ID: NCT05355441

Last Updated: 2025-02-12

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

38 participants

Study Classification

OBSERVATIONAL

Study Start Date

2022-04-01

Study Completion Date

2024-11-01

Brief Summary

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In Spain, major trauma continues to be the leading cause of death among young people. However, mortality rates represent only a relatively small part of the impact of trauma injuries on the health of the population. Pain and anxiety are two of the most poorly controlled factors that have a huge impact on a patient's quality of life.The type of therapy that has been shown to be most effective in treating post-traumatic pain is one that involves different specialists, given its multicausality, care should be multidisciplinary.

This investigation project consists in an observational study performed by a multidisciplinary team in our center. Major trauma patients with moderate, severe or incapacitating pain will be referred to consultations specialized in chronic pain and psychology. One year after the trauma, patients will be evaluated in terms of quality of life.

The aim of this study is to determinate the impact that multidisciplinary treatment of post-traumatic pain has on the perception of quality of life in severely injured patients.

Detailed Description

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Conditions

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Trauma Chronic Pain Psychological Trauma

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Multidisciplinar pain treatment patients

Major trauma patients with moderate, severe or incapacitating pain will be referred to consultation specialized in chronic pain and psychology. Patients will be evaluated, in terms of quality of life, before and after the treatment.

Paracetamol

Intervention Type DRUG

Routine clinical practice treatments recommended by the medical team involved

Ibuprofen 600 mg

Intervention Type DRUG

Routine clinical practice treatments recommended by the medical team involved

Tramadol

Intervention Type DRUG

Routine clinical practice treatments recommended by the medical team involved

Morphine

Intervention Type DRUG

Routine clinical practice treatments recommended by the medical team involved

Interventions

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Paracetamol

Routine clinical practice treatments recommended by the medical team involved

Intervention Type DRUG

Ibuprofen 600 mg

Routine clinical practice treatments recommended by the medical team involved

Intervention Type DRUG

Tramadol

Routine clinical practice treatments recommended by the medical team involved

Intervention Type DRUG

Morphine

Routine clinical practice treatments recommended by the medical team involved

Intervention Type DRUG

Other Intervention Names

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Psychological drugs Psychological drugs Psychological drugs Psychological drugs

Eligibility Criteria

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Inclusion Criteria

* Major trauma patients with moderate, severe or incapacitating pain (according to EQ-5D-5L scale).

Exclusion Criteria

* Death in the first 30 days after the trauma.
* Transferred to another center.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Corporacion Parc Tauli

OTHER

Sponsor Role collaborator

Nuria Llorach-Perucho

OTHER

Sponsor Role lead

Responsible Party

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Nuria Llorach-Perucho

Principal Investigator

Responsibility Role SPONSOR_INVESTIGATOR

Principal Investigators

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Nuria Llorach-Perucho, MD

Role: PRINCIPAL_INVESTIGATOR

Corporacion Parc Tauli

Salvador Navarro-Soto, MD, PhD

Role: STUDY_DIRECTOR

Corporacion Parc Tauli

Heura Llaquet-Bayo, MD, PhD

Role: STUDY_DIRECTOR

Corporacion Parc Tauli

Locations

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Corporació Sanitària Parc Taulí

Sabadell, Barcelona, Spain

Site Status

Countries

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Spain

Other Identifiers

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DOLOTRAU

Identifier Type: -

Identifier Source: org_study_id

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