NCT01547663

Unknown

A Comparison of Pain Scales in Patients With Disorder of Con...

Mahidol University Source

Other study identifiers

Sponsor study identifier

SIRB 461/2554

Study Type

observational

Estimated enrollment

40

Locations

1 country

Sites

1

Timeline

Study Start

March 2012

Date type not reported

This date has not been verified as actual or estimated.

Primary Completion

October 2013

Estimated (date passed)

This estimate has passed. The registry has not confirmed an actual date for this milestone.

Study Completion

December 2013

Estimated (date passed)

This estimate has passed. The registry has not confirmed an actual date for this milestone.

Brief Summary

This study aims to test validity, reliability and practicality of translated NCS, CNPI and FLACC in unconscious patients in 48 hour following craniotomy.

Registry Overview

Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.

Recruitment status: unknown
Estimated enrollment: 40 participants
Study completion date: December 2013
Estimated (date passed)
This estimate has passed. The registry has not confirmed an actual date for this milestone.
Listed locations: 1 countries · 1 sites

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.

Study Start
March 2012
Date type not reported
This date has not been verified as actual or estimated.
First Submitted
March 4, 2012
Actual (reported)
First Posted
March 8, 2012
Actual (reported)
Primary Completion
October 2013
Estimated (date passed)
This estimate has passed. The registry has not confirmed an actual date for this milestone.
Study Completion
December 2013
Estimated (date passed)
This estimate has passed. The registry has not confirmed an actual date for this milestone.

Last Updated: March 8, 2012
Status Verified: March 2012
Last Update Submitted: March 7, 2012

Conditions

Pain, Postoperative

Keywords

pain scalecraniotomy

Eligibility Criteria

Age18 Years - 80 Years

Sexall

Healthy VolunteersNo

Age GroupsAdult (18-64), Older Adult (65+)

Sampling MethodNon-Probability Sample

Study Population

patients with disorder of consciousness within 48 hours following craniotomy

You may qualify if:

Age \> 18 years old
Preoperative intracranial lesion which predicts delayed recovery
Disorder of consciousness within 48 hours after craniotomy assessed by using Coma Recovery Scale-Revised (CRS-R) 17
Not received postoperative sedation or muscle relaxants

You may not qualify if:

Sponsors & Collaborators

Mahidol University
Otherlead

Study Sites (1)

Siriraj Hospital, Mahidol University

Bangkok, Bangkok, 10700, Thailand

Suwannee Suraseranivongse, MDCONTACT66814087655 sisur@mahidol.ac.th

Suwannee Suraseranivongse, MDPRINCIPAL INVESTIGATOR

MeSH Terms

Conditions

Pain, Postoperative

Condition Hierarchy (Ancestors)

Postoperative ComplicationsPathologic ProcessesPathological Conditions, Signs and SymptomsPainNeurologic ManifestationsSigns and Symptoms

Study Design

Study Type: observational
Observational Model: CASE ONLY
Time Perspective: PROSPECTIVE
Sponsor Type: OTHER
Responsible Party: PRINCIPAL INVESTIGATOR
PI Title: Professor

Study Record Dates

First Submitted

March 4, 2012

First Posted

March 8, 2012

Study Start

March 2012

Date type not reported

This date has not been verified as actual or estimated.

Primary Completion

October 2013

Estimated (date passed)

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Phase 2Unknown

Documented history of prior brain injury

History of delayed development

Prior psychiatric illness

Prior neurological illness

Superior limb contusion, fracture, paralysis -cannot move

Thalamic hemorrhage -cannot express feeling

Contact the study team to confirm eligibility.

This estimate has passed. The registry has not confirmed an actual date for this milestone.

Study Completion

December 2013

Estimated (date passed)

This estimate has passed. The registry has not confirmed an actual date for this milestone.

Last Updated

March 8, 2012

Record last verified: 2012-03

Source record

Download the complete ClinicalTrials.gov record imported by Syfrah, including fields not shown in this page. The registry may contain a newer revision.

Source: ClinicalTrials.gov.

JSON downloads include source attribution and retrieval details alongside the unchanged original record or the separately normalized values.

Registry identifier: NCT01547663
Data provider: ClinicalTrials.gov
Source updated: 2012-03-08
Normalization version: ctgov-legacy-1

Open registry record

Source retrieved: 2026-10-25 22:39:41 UTC

Locations

TH(1)

Brief Summary

Registry Overview

Trial Relationships

Related Scientific Literature

Study Timeline

Study Start

First Submitted

First Posted

Primary Completion

Study Completion

Conditions

Keywords

Eligibility Criteria

You may qualify if:

You may not qualify if:

Sponsors & Collaborators

Study Sites (1)

MeSH Terms

Conditions

Condition Hierarchy (Ancestors)

Study Design

Study Record Dates

Source record

Locations