Evaluating the Efficacy of Intranasal Oxytocin on Chronic Pain

PHASE2/PHASE3RecruitingINTERVENTIONAL
Enrollment

336

Participants

Timeline

Start Date

April 1, 2022

Primary Completion Date

March 31, 2026

Study Completion Date

March 31, 2026

Conditions
Chronic Pain
Interventions
DRUG

24-IU oxytocin

Patients will self-administer a 2-week course of 24-IU intranasal oxytocin \[4-IU per puff (12-IU delivered to each nostril); Syntocinon, Novartis, Switzerland\], twice per day (once in the morning and once in the evening).

DRUG

48-IU oxytocin

Patients will self-administer a 2-week course of 48-IU intranasal oxytocin \[4-IU per puff (24-IU delivered to each nostril); Syntocinon, Novartis, Switzerland\], twice per day (once in the morning and once in the evening).

DRUG

Placebo

Patients will receive an intranasal placebo containing the same ingredients as the oxytocin nasal spray with the exception of active oxytocin. Administration schedule and procedure will be identical to that described in 24-IU oxytocin.

Trial Locations (3)

T2T 5C7

RECRUITING

Calgary Chronic Pain Centre, Calgary

V3T0G9

RECRUITING

Jim Pattison Outpatient Care & Surgical Centre Pain Clinic (JPOCSC-PC), Surrey

A1Y 1A4

RECRUITING

Carbonear General Hospital, Carbonear

All Listed Sponsors
collaborator

University of Calgary

OTHER

collaborator

University of British Columbia

OTHER

lead

Memorial University of Newfoundland

OTHER