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Status unknownNCT05702125Updated Jan 27, 2023

Chronic Pain After Cardiothoracic Surgery

An observational study in Chronic Pain, Thoracic and Chronic Pain Syndrome, sponsored by Indonesia University. Status unknown. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2023-01-27.

Sponsored by Indonesia University · Observational

The sponsor has not verified this record recently (last verified Jan 2023), so the status shown — last known as Not yet recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
96
Ages
18 Years and older
Sex
All
01

Study summary

This is a prospective cohort study to estimate prevalence of chronic pain after cardiothoracic surgery

Read the detailed description

This is a prospective cohort study of all patients undergo cardiothoracic elective surgery in Cipto Mangunkusumo Hospital using general anesthesia. Patients with emergency surgery, history of psychologic and neurologic disease which cannot reliably state their pain score, cannot communicate well, and disagree to follow the research will be exempted. The pain score will be recorded one week after surgery during walk-in consultation, followed by 3 months and 6 months after surgery via telecommunication.

02

Conditions studied

  • Chronic Pain
  • Thoracic
  • Chronic Pain Syndrome

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Keywords

  • chronic pain
  • thoracotomy
  • sternotomy
  • cardiothoracic surgery
03

In context

Chronic Pain

2,930 studies on the registry are indexed under Chronic Pain; 701 are open to participants now.

This study's planned enrollment of 96 is below the median of 126 across 688 observational studies indexed under Chronic Pain.

Browse Chronic Pain studies →

Lead sponsor

Indonesia University is the lead sponsor of 448 studies on the registry; 56 are open to participants now.

Of its 6 completed or terminated interventional studies of FDA-regulated products, 1 (17%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients undergo elective sternotomy and/or thoracotomy using general anesthesia in Cipto Mangunkusumo hospital during January 2023 until March 2024

Inclusion criteria

  • Patients undergo elective sternotomy and/or thoracotomy using general anesthesia
  • Patients agree to follow the study

Exclusion criteria

Exclusion Criteria:

  • Patients undergo emergency sternotomy or thoracotomy
  • Patients with pyschological and neurological disorder, that it is not reliable to determine the pain intensity
  • Patients who cannot communicate
  • Patients disagree to follow the study
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
96 participants (estimated)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Visual Analog Scale

    Pain score to assess pain intensity

    Time frame: 1 week after surgery

  2. Visual Analog Scale

    Pain score to assess postoperative pain intensity

    Time frame: 3 months after surgery

  3. Visual Analog Scale

    Pain score to assess postoperative pain intensity

    Time frame: 6 months after surgery

07

Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 27, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT05702125
Lead sponsor
Indonesia University
Responsible party
Ratna Farida Soenarto (Principal Investigator, Indonesia University) — Principal investigator
First posted
Jan 27, 2023
Start date
Feb 1, 2023 (estimated)
Primary completion
Mar 31, 2024 (estimated)
Completion
Mar 31, 2024 (estimated)
Last update
Jan 27, 2023

Study contacts

Ratna F Soenarto, Consultant
Contact
fida.soenarto@gmail.com
81310538988 ext. +62
Ratna F Soenarto, Consultant
principal investigator · Indonesia University

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jan 2023. You cannot join it, but the record below documents what was studied.

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