Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04866147
Other study ID # CPSP001122
Secondary ID
Status Completed
Phase
First received
Last updated
Start date May 25, 2021
Est. completion date August 15, 2023

Study information

Verified date October 2023
Source University of Aarhus
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This research will be a prospective single-centre observational cohort study in Denmark spanning approximately one year. The objective of this study is to develop a clinically applicable and generalizable prediction model for postsurgical pain in adults.


Recruitment information / eligibility

Status Completed
Enrollment 1522
Est. completion date August 15, 2023
Est. primary completion date May 15, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Consenting Danish-speaking adults aged 18 years and older - Patients who undergo common inpatient or outpatient surgical procedures Exclusion Criteria: - Patients with cognitive impairment - Patients who refuse or unable to provide informed consent - Patients who undergo re-operation within 3 months of their initial surgery

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Cardiothoracic surgery
Cardiac & large intrathoracic vessels, respiratory, thoracic, mediastinal & diaphragmatic procedures
Breast surgery
Breast resections & mastectomies
Gastrointestinal surgery
Digestive & spleen
Genitourinary surgery
Urinary tract, genital & retroperitoneal tissue
Orthopaedic surgery
Back & neck, shoulder & upper arm, hip & thigh, knees & lower leg

Locations

Country Name City State
Denmark Aarhus University Hospital Aarhus N
Denmark Silkeborg Regional Hospital Silkeborg

Sponsors (1)

Lead Sponsor Collaborator
University of Aarhus

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Chronic post surgical pain Pain related to the surgical procedure measured as average pain intensity on rest or movement using 11-point numeric rating scale (NRS; 0-10) where 0=no pain and 10=worst pain imaginable and/or average pain interference using 11-point NRS among any one of seven short-form Brief Pain Inventory items (general activity, mood, walking ability, normal work (including housework), relations with other people, sleep, enjoyment of life) in the past one week, where 0=pain does not interfere and 10=pain completely interferes. 3 months post surgery
Secondary Acute post surgical pain Acute post surgical pain intensity in the first 3 hours after surgery measured as pain at rest using 11-point numeric rating scale (NRS; 0-10) where 0=no pain and 10=worst pain imaginable. First 3 hours after surgery
See also
  Status Clinical Trial Phase
Recruiting NCT05572307 - Peripheral Blood Single Cell Sequencing Analysis of POD and CPSP in Elderly Patients After Total Knee Arthroplasty
Not yet recruiting NCT06062550 - Different Dose Esketamine and Dexmedetomidine Combination for Supplemental Analgesia After Scoliosis Correction Surgery Phase 4
Completed NCT04924010 - Effect of Perioperative CBT on Chronic Persistent Postsurgical Pain Among Breast Cancer Patients N/A
Completed NCT05364216 - Effect of TPVB on Postoperative Pain and Cognitive Function After VATS in Elderly Patients N/A
Recruiting NCT06374849 - Intraoperative Sufentanil and Chronic Postsurgical Pain in Non-major Scheduled Abdominal Surgery Phase 4
Not yet recruiting NCT06083480 - Reducing Perioperative Oxidative Stress to Prevent Postoperative Chronic Pain Following Total Knee Arthroplasty Phase 4
Recruiting NCT05037123 - Optimizing the Use of Ketamine to Reduce Chronic Postsurgical Pain Phase 3
Active, not recruiting NCT05718544 - Mini-dose Esketamine-dexmedetomidine Supplemented Analgesia and Long-term Outcomes Phase 4
Not yet recruiting NCT06087510 - Different Dose Esketamine and Dexmedetomidine for Supplemental Analgesia and Longterm Outcomes Phase 4
Recruiting NCT05196503 - Efficacy of an Intraoperative Periradicular Application of Platelet Rich Fibrin (PRF) on the Intensity of Residual Post-surgical Neuropathic Pain After a Surgery for Disc Herniation Phase 3
Not yet recruiting NCT06126289 - CSF Single-cell Sequencing and Proteomics of Chronic Postsurgical Pain in Patients With Lower Limb Fractures
Recruiting NCT05160493 - The Effect of Esketamine Combined With Pregabalin on Chronic Postsurgical Pain in Patients After Craniotomy. Phase 2/Phase 3
Completed NCT01537731 - Vaginal or Laparoscopic Hysterectomy, Persistent Postsurgical Pain N/A
Completed NCT05372406 - Clinical Prediction Model and External Validation of Chronic Postsurgical Pain in Elders
Recruiting NCT03847363 - The Influence of Different Anesthesia on Acute and Chronic Postsurgical Pain After Thoracic Surgery