NCT00314392

Brief Summary

The response to standard pain stimuli in males and females is investigated, together with the effect of informing participants about the effect of a painkiller. Physiological response to pain is recorded.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
74

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Sep 2006

Geographic Reach
1 country

1 active site

Status
completed

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

First Submitted

Initial submission to the registry

April 11, 2006

Completed
2 days until next milestone

First Posted

Study publicly available on registry

April 13, 2006

Completed
5 months until next milestone

Study Start

First participant enrolled

September 1, 2006

Completed
1.2 years until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2007

Completed
Last Updated

February 6, 2008

Status Verified

February 1, 2008

First QC Date

April 11, 2006

Last Update Submit

February 4, 2008

Conditions

Experimental Pain

Keywords

Experimental painPlacebo analgesiaHeart rate variabilitySkin conductance

Outcome Measures

Primary Outcomes (1)

  • Pain report, heart rate variability, skin conductance

Secondary Outcomes (1)

  • Subjective arousal

Interventions

Information (behavior)BEHAVIORAL

Eligibility Criteria

Age18 Years - 40 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • years, healthy

You may not qualify if:

  • pregnant, earlier serious disease or injury,

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University Hospital of North Norway

Tromsø, Troms, N-9038, Norway

Location

Study Officials

  • Magne Arve Flaten, PhD

    University of Tromso

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER

Study Record Dates

First Submitted

April 11, 2006

First Posted

April 13, 2006

Study Start

September 1, 2006

Study Completion

December 1, 2007

Last Updated

February 6, 2008

Record last verified: 2008-02

Locations

NO(1)