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Comparison of Treatment Effects of PowerScope2 and Forsus Using CBCT

NCT03296644 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 42

Last updated 2019-04-29

No results posted yet for this study

Summary

The main objective of this prospective, controlled clinical study is:

1. To compare the treatment effects of PowerScope2 and Forsus Fatigue Resistant Device in patients with Class II divison1 malocclusion.
2. To compare the treatment effects of PowerScope2 and Forsus Fatigue Resistant Device with the control group.

The null hypothesis for this study is that Forsus and PowerScope2 are equally effective in the treatment of ClassII div1 malocclusion.

Conditions

  • Class II Division 1 Malocclusion

Interventions

DEVICE

Class II correction using PowerScope2

DEVICE

Class II correction using Forsus

Sponsors & Collaborators

  • Postgraduate Institute of Dental Sciences Rohtak

    lead OTHER

Principal Investigators

  • Sonal Chowdhary · POST GRADUATE INSTITUTE OF DENTAL SCIENCES

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
12 Years
Max Age
17 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-08-16
Primary Completion
2018-04-30
Completion
2018-04-30

Countries

  • India

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03296644 on ClinicalTrials.gov