NCT02498184

Brief Summary

This is a double-blinded, randomized, controlled study on the effect of perioperative acupuncture on pain after third molar extraction.

Trial Health

43
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
100

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Nov 2016

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
unknown

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

July 13, 2015

Completed
2 days until next milestone

First Posted

Study publicly available on registry

July 15, 2015

Completed
1.3 years until next milestone

Study Start

First participant enrolled

November 1, 2016

Completed
2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2018

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

November 1, 2018

Completed
Last Updated

November 28, 2017

Status Verified

November 1, 2017

Enrollment Period

2 years

First QC Date

July 13, 2015

Last Update Submit

November 27, 2017

Conditions

Outcome Measures

Primary Outcomes (1)

  • pain scale

    24 hours

Study Arms (2)

real acupuncture

EXPERIMENTAL

traditional chinese acupuncture

Other: acupuncture

sham acupuncture

SHAM COMPARATOR

non effective acupuncture

Other: acupuncture

Interventions

real acupuncturesham acupuncture

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Ziv Medical Center

Safed, 1008, Israel

RECRUITING

MeSH Terms

Interventions

Acupuncture Therapy

Intervention Hierarchy (Ancestors)

Complementary TherapiesTherapeutics

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
TRIPLE
Who Masked
PARTICIPANT, CARE PROVIDER, OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER GOV
Responsible Party
SPONSOR

Study Record Dates

First Submitted

July 13, 2015

First Posted

July 15, 2015

Study Start

November 1, 2016

Primary Completion

November 1, 2018

Study Completion

November 1, 2018

Last Updated

November 28, 2017

Record last verified: 2017-11

Locations