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Clonidine-Remifentanil. Effect of the Combination on Acute Pain and Respiration in Healthy Volunteers (Remiclon)

University of Oslo (UIO) logo

University of Oslo (UIO)

Status and phase

Completed
Phase 2
Phase 1

Conditions

Respiration
Sedation
Acute Pain

Treatments

Drug: Remifentanil+clonidine

Study type

Interventional

Funder types

Other

Identifiers

NCT00730054
S-03025

Details and patient eligibility

About

The hypothesis is that systemic remifentanil and Clonidine act in a synergistic manner to relief acute main in an experimental human pain model. Of interest is also the effect of the combination on respiration, sedation and cognitive behavior.

Full description

To examine the possible synergistic effects og systemic remifentanil and clonidine. Its effects on respiration, cognitive function and sedation.

Enrollment

12 patients

Sex

All

Ages

18 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Healthy volunteers

Exclusion criteria

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Triple Blind

12 participants in 4 patient groups, including a placebo group

1
Active Comparator group
Description:
Clonidine
Treatment:
Drug: Remifentanil+clonidine
2
Active Comparator group
Description:
Remifentanil
Treatment:
Drug: Remifentanil+clonidine
4
Experimental group
Description:
Remifentanil+clonidine
Treatment:
Drug: Remifentanil+clonidine
3
Placebo Comparator group
Description:
Placebo
Treatment:
Drug: Remifentanil+clonidine

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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