Dextromethorphan Effect on Central Sensitization to Pain in Healthy Volunteers

Hyperalgesia Clinical Trial

— Hydex  

Official title:

Dextromethorphan Effect on Central Sensitization to Pain in Healthy Volunteers

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02596360
• Other study ID #: CHU-0248
• Secondary ID: 2015-003271-30
• Status: Completed
• Phase: Phase 1
• First received: October 19, 2015
• Last updated: March 31, 2016
• Start date: November 2015
• Est. completion date: March 2016

Study information

• Verified date: March 2016
• Source: University Hospital, Clermont-Ferrand
• Contact: n/a
• Is FDA regulated: No
• Health authority: France: Agence Nationale de Sécurité du Médicament et des produits de santé
• Study type: Interventional

Clinical Trial Summary

The aim of this study is to assess the anti-hyperalgesic effect of dextromethorphan in healthy volunteers compared to placebo.

Description:

This is a cross-over group, double-blind, randomized clinical trial in healthy volunteers comparing dextromethorphan and inactive control on freeze-induced hyperalgesia, experimental pain, diffuse noxious inhibitory control (DNIC), pupillary reaction and reaction time.

The influence of CYP3A4 and MDR1 polymorphism on the dextromethorphan analgesic efficacy will be measured.

The study design is divided in two study sequences and each subject participates in the two study sequences and receive the two treatments (dextromethorphan and placebo).

Each study sequence consists of 3 assessment days (Day -1, Day 0 = first treatment administration and Day 1).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 20
• Est. completion date: March 2016
• Est. primary completion date: March 2016
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Male
• Age group: 18 Years to 45 Years

Eligibility

Inclusion Criteria:

• Healthy male volunteers

• Aged between 18 and 45 years

• CYP2D6 Extensive and Intermediate metabolizers

• Body mass index (BMI) between 19 and 30 kg/m2

• Systolic blood pressure between 100 and 150 mmHg, diastolic blood pressure between 50 and 90 mmHg, heart rate between 45 and 90 beats per minute

• Without treatment during the 7 days before inclusion specially no use of analgesic and anti-inflammatory drugs

• Cooperation and understanding enough to conform to the study obligations

• Having given free informed written consent

• Affiliated to the French Social Security

• Inscription or acceptation of inscription in the national register of volunteers involved in trials.

Exclusion Criteria:

• Hypersensitivity to the active substance or to any of the excipients

• Lactose intolerance

• Hypertension

• History of stroke

• Severe heart failure

• Severe hepatic impairment

• Shortness of breath

• Congenital galactosemia, glucose-galactose malabsorption, lactase deficiency

• Association with linezolid

• Pre-existence or history of peripheral neuropathy due to a cause different from neurotoxic chemotherapy

• Diabetes (type I and II)

• CYP2D6 Poor and Ultra-rapid metabolizers

• AST, ALT, total bilirubin twice the average

• Dextromethorphan intake during the 7 days before inclusion

• Medical and surgical history incompatible with the study

• Disease progression during inclusion

• Excessive consumption of alcohol (> 50g/day), tobacco (= 10 cigarettes/day), coffee, tea or drinks with caffeine (equivalent to more than 4 cups a day) or any addiction to drugs

• Subject lacking concentration during tests training and low test results reproducibility

• Subject does not meet the selection criteria for its ability to discriminate sensations to noxious stimuli during psychometric tests

• Subject exclusion period, or the total allowable compensation exceeded

• Subject undergoing a measure of legal protection (guardianship, supervision

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Experimental Pain
• Hyperalgesia

Intervention

Drug:
• Pulmodexane® 30mg
The study design is divided in two study sequences and each subject participates in the two study sequences and receive the two treatments (dextromethorphan and placebo).
• lactose
The study design is divided in two study sequences and each subject participates in the two study sequences and receive the two treatments (dextromethorphan and placebo).

Locations

Country	Name	City	State
France	CHU Clermont-Ferrand	Clermont-Ferrand

Sponsors (1)

Lead Sponsor	Collaborator
University Hospital, Clermont-Ferrand

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Area under the curve (AUC) of percentage changes in mechanical pain thresholds (MPT) using electronic von frey in secondary hyperalgesic zone (Z2)		at Day 0 after treatment administration: 1 hour post-dose (T0+1h), 2 hours post-dose (T0+2h) and 3 hours post-dose (T0+3h).	No
Secondary	Area under the curve (AUC) of percentage changes in mechanical pain thresholds (MPT) using electronic von frey in control skin zone (Z0) and primary hyperalgesic zone (Z1)		at D0 T0+1h, T0+2h and T0+3h after treatment administration	No
Secondary	Percentage changes in mechanical pain thresholds (MPT) using electronic von frey in control skin zone (Z0)		at Day 0 after treatment administration: 1 hour post-dose (T0+1h), 2 hours post-dose (T0+2h) and 3 hours post-dose (T0+3h).	No
Secondary	Percentage changes in mechanical pain thresholds (MPT) using electronic von frey in primary hyperalgesic zone (Z1)		at Day 0 30 min before treatment (T0-30min ) and at Day 0 after treatment administration: 1 hour post-dose (T0+1h), 2 hours post-dose (T0+2h) and 3 hours post-dose (T0+3h) and at Day 1 after treatment administration: 24,5 hours post-dose (T0+24h30).	No
Secondary	Conditioned Pain Modulation (CPM) assessment		at Day -1 before treatment and Day 0 30 min before treatment (T0-30min)	No
Secondary	Reaction time assessment using RTI CANTAB® test		at Day -1 before treatment and Day 0 30 min before treatment (T0-30min), after treatment administration: 1 hour post-dose (T0+1h) and 3 hours post-dose (T0+3h) and at Day 1 after treatment administration: 24,5 hours post-dose (T0+24h30).	No
Secondary	Determination of potential central effects of dextromethorphan measuring pupillary reaction	Determination of potential central effects of dextromethorphan measuring pupillary reaction assessing the diameter of the pupil in real time in scotopic conditions (e.g. size variation [mm]; contraction speed [mm.s-1]; contraction latency [ms]) at Day 0 30 min before treatment (T0-30min ) and at Day 0 after treatment administration: 1 hour post-dose (T0+1h), 2 hours post-dose (T0+2h) and 3 hours post-dose (T0+3h) and at Day 1 after treatment administration: 24,5 hours post-dose (T0+24h30).; - Study of genetic polymorphism of cytochrome P450 3A4 and MDR1 gene through study completion, up to 6 months.	at Day 0 30 min before treatment (T0-30min ) and at Day 0 after treatment administration: 1 hour post-dose (T0+1h), 2 hours post-dose (T0+2h) and 3 hours post-dose (T0+3h) and at Day 1 after treatment administration: 24,5 hours post-dose (T0+24h30).	No
Secondary	Study of genetic polymorphism of cytochrome P450 3A4 and genetic polymorphism of MDR1 gene		up to 6 months.	No
Secondary	Dosage of plasma concentration of dextromethorphan and dextromethorphan's metabolites from blood collections		at Day 0 30 min before treatment (T0-30min ) and at Day 0 after treatment administration: 2 hours post-dose (T0+2h) and at Day 1 after treatment administration: 24,5 hours post-dose (T0+24h30).	No