NCT00199316

Brief Summary

postoperative pain after kidney surgery is very high. We always use PCA for postopertive pain. But almost patients still had severe pain. We try to use spinal morphine before operation aims to reduce pain.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
80

participants targeted

Target at P50-P75 for not_applicable postoperative-pain

Timeline
Completed

Started Jan 2005

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2005

Completed
9 months until next milestone

First Submitted

Initial submission to the registry

September 14, 2005

Completed
6 days until next milestone

First Posted

Study publicly available on registry

September 20, 2005

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

November 1, 2005

Completed
Last Updated

March 21, 2018

Status Verified

October 1, 2007

First QC Date

September 14, 2005

Last Update Submit

March 19, 2018

Conditions

Postoperative Pain

Keywords

patient who recieve kidney surgery and Patient controlled anesthesia with spinal morphine, intrathecal

Outcome Measures

Primary Outcomes (1)

  • pain score

    48 hours

Secondary Outcomes (2)

  • morphine consumption in PCA

    48 hours

  • side effect

    48 hours

Interventions

spinal morphineDRUG

Eligibility Criteria

Age15 Years - 60 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64)

You may qualify if:

  • kidney surgery who less than 60 years old.
  • no underlying disease
  • ASA less than 3

You may not qualify if:

  • refuse spinal morphine
  • history of morphine allery

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Khon Kaen university, Srinagarind Hospital

Muang, Changwat Khon Kaen, 40002, Thailand

RECRUITING

MeSH Terms

Conditions

Pain, Postoperative

Condition Hierarchy (Ancestors)

Postoperative ComplicationsPathologic ProcessesPathological Conditions, Signs and SymptomsPainNeurologic ManifestationsSigns and Symptoms

Study Officials

  • Polpun Boonmak, MD

    lecturer in Khon Kaen University

    STUDY DIRECTOR

Central Study Contacts

Polpun Boonmak, MD

CONTACT

polpun@hotmail.com

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
QUADRUPLE
Who Masked
PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER

Study Record Dates

First Submitted

September 14, 2005

First Posted

September 20, 2005

Study Start

January 1, 2005

Study Completion

November 1, 2005

Last Updated

March 21, 2018

Record last verified: 2007-10

Locations

TH(1)