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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01594775
Other study ID # KEK-ZH-NR: 2009-0063
Secondary ID
Status Completed
Phase Phase 1
First received May 7, 2012
Last updated February 24, 2014
Start date October 2011
Est. completion date October 2013

Study information

Verified date February 2014
Source University of Zurich
Contact n/a
Is FDA regulated No
Health authority Switzerland: Swissmedic
Study type Interventional

Clinical Trial Summary

effects of intranasal oxytocin and couple interaction on wound healing.

- Trial with medicinal product


Recruitment information / eligibility

Status Completed
Enrollment 160
Est. completion date October 2013
Est. primary completion date October 2013
Accepts healthy volunteers No
Gender Both
Age group 21 Years to 45 Years
Eligibility Inclusion criteria:

- healthy heterosexual couples

- in a stable relationship since > 1 year

Exclusion criteria: pregnancy

- breast feeding

- heavy smoking (> 5 cigarettes/d)

- extensive skin disease

- artificial UV irradiation during < 3 months before study inclusion

Study Design

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


Related Conditions & MeSH terms


Intervention

Drug:
Syntocinon (Oxytocin) nasal spray
two-times daily self-administration of nasal spray containing active substance (oxytocin) during five days after wounding.
Placebo
two-times daily self-administration of nasal spray containing placebo during five days after wounding.

Locations

Country Name City State
Switzerland University Hospital Zurich, Dept. of Dermatology Zurich

Sponsors (2)

Lead Sponsor Collaborator
University of Zurich Swiss National Science Foundation

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary wound size wound healing process within seven days after wounding seven days No
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