CompletedNot Applicable

Comparison of Treatment Effects of PowerScope2 and Forsus Using CBCT

India42 participantsStarted 2016-08-16

Plain-language 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.

Who can participate

Age range

12 Years – 17 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Patients in active growth period * Skeletal Class II malocclusion * Normal or mildly prognathic maxilla * Retrognathic mandible. * Increased overjet, not less than 5 mm. * Horizontal to average growth pattern * Positive pretreatment visual treatment objective (VTO). * Minimum crowding in dental arches. * Treatment completed without any permanent teeth extracted (excluding third molars). Exclusion Criteria:• Subjects with a history of orthodontic treatment * Anterior open bite * Severe proclination and crowding of anterior teeth * Any systemic disease affecting bone and generalgrowth * Vertical growth pattern * Patient who fails to follow up or undergo complete treatment

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

mandibular length

Timeframe: 20 months

oropharyngeal volume

Timeframe: 20 months

condylar changes

Timeframe: 20 months

patient experiences

Timeframe: 20 months

pancherz analysis

Timeframe: 20 months

soft tissue changes

Timeframe: 20 months

Trial details

NCT IDNCT03296644

SponsorPostgraduate Institute of Dental Sciences Rohtak

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2018-04

View on ClinicalTrials.gov More Class II Division 1 Malocclusion trials

Plain-language summary

Who can participate

Age range

12 Years – 17 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.