ClinicalTrials.gg
RecruitingNCT07773389Updated Aug 19, 2026

Effect of Early Versus Late Premolar Extraction on Orthodontic Tooth Movement

An interventional study of Early Maxillary First Premolar Extraction and Late Maxillary First Premolar Extraction in Malocclusion Class II and Malocclusion, Angle Class I, sponsored by Shifa College of Dentistry. Recruiting at 1 site in Pakistan. Open to participants aged 13 Years to 25 Years. Per ClinicalTrials.gov, last updated 2026-08-19.

Sponsored by Shifa College of Dentistry · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Started Jul 2026; still recruiting 3 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
26
Allocation
Randomized
Ages
13 Years to 25 Years
Sex
All
01

Study summary

The goal of this randomized controlled trial is to evaluate whether the timing of premolar extraction affects the rate of orthodontic space closure during en-masse anterior retraction. The study will also assess gingival cleft formation, mesial movement of the upper first molars, ease and duration of premolar extraction, and patient-reported pain and anxiety.

The main question it aims to answer is:

Does early versus late premolar extraction affect the rate of orthodontic space closure?

Researchers will compare two groups of patients. In the early extraction group the maxillary first premolars will be extracted before or within one week of start of fixed orthodontic treatment. In the late extraction group, the premolars will be extracted after alignment and immediately before the start of space closure.

Participants will:

  • Receive fixed orthodontic treatment and bilateral extraction of the maxillary first premolars.
  • Be randomly assigned to either the early-extraction or late-extraction group.
  • Undergo orthodontic alignment followed by en-masse anterior retraction.
  • Have dental impressions/digital models obtained at the start of retraction and at 3 and 6 months to measure orthodontic tooth movement and space closure.
  • Be assessed for gingival clefts and mesial movement of the upper first molars.
  • Have the ease and duration of their premolar extraction recorded and report their pain and anxiety associated with the extraction procedure.
Read the detailed description

This randomized controlled trial will evaluate the effect of early versus late maxillary first premolar extraction on the rate of orthodontic space closure during en-masse anterior retraction. A total of 26 participants aged 13 to 25 years requiring bilateral maxillary first premolar extractions as part of their orthodontic treatment will be randomly allocated in a 1:1 ratio to an early-extraction or late-extraction group.

In the early-extraction group, the maxillary first premolars will be extracted before or within one week of fixed appliance placement. Participants will subsequently undergo leveling and alignment, and en-masse anterior retraction will begin after stabilization on a 0.019 × 0.025-inch stainless steel archwire. In the late-extraction group, leveling and alignment will be completed first using the same archwire sequence. The maxillary first premolars will then be extracted immediately before initiation of en-masse anterior retraction. Thus, space closure will occur through relatively healed extraction sites in the early-extraction group and relatively fresh extraction sites in the late-extraction group.

Orthodontic space closure will be assessed at baseline and at 3 and 6 months after initiation of retraction. Secondary assessments will include mesial movement of the maxillary first molars, incidence and severity of gingival clefts, ease and duration of premolar extraction, and patient-reported pain and anxiety. Digital models will be used to assess orthodontic tooth movement, while gingival clefts will be evaluated clinically.

02

Conditions studied

  • Malocclusion Class II
  • Malocclusion, Angle Class I

Keywords

  • Orthodontic Tooth movement
  • Premolar extraction
  • Early Extraction
  • Late Extraction
  • Orthodontic Space Closure
  • En-masse anterior retraction
  • Gingival Cleft
  • Anchorage loss
03

In context

Malocclusion, Angle Class I

35 studies on the registry are indexed under Malocclusion, Angle Class I; 10 are open to participants now.

This study's planned enrollment of 26 is below the median of 32 across 31 interventional studies indexed under Malocclusion, Angle Class I.

Browse Malocclusion, Angle Class I studies →

Lead sponsor

Shifa College of Dentistry is the lead sponsor of 2 studies on the registry; 2 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
13 Years to 25 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Age 13-25 years
  2. No prior orthodontic treatment
  3. Overjet 4-8 mm
  4. Symmetric dental arches with mild to moderate crowding requiring bilateral first premolar extractions.
  5. Probing depth less than 4 mm on all teeth

Exclusion criteria

Exclusion Criteria:

  1. History of dental trauma
  2. Poor oral hygiene
  3. Syndromic patients
  4. Systemic diseases or medications affecting bone metabolism
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
26 participants (estimated)

Study arms

  • Active comparator
    Healed Socket Group (Control Group)

    Maxillary first premolars will be extracted before or within one week of fixed orthodontic appliance placement. Participants will subsequetly undergo leveling and alignment followed by en-masse anterior retraction after stabilization on a 0.019 x 0.025-inch stainless steel archwire.

    Procedure: Early Maxillary First Premolar Extraction

  • Experimental
    Unhealed Socket Group (Intervention Group)

    Maxillary first premolars will be extracted after the participant has completed leveling and alignment, and has been stabilizad on a 0.019 x 0.025-inch stainless steel archwire for one month. This will be followed immediately by en-masse anterior retraction.

    Procedure: Late Maxillary First Premolar Extraction

Interventions

  • ProcedureEarly Maxillary First Premolar Extraction

    Bilateral extraction of the maxillary first premolars will be performed prior to or within one week of fixed orthodontic appliance placement, allowing the extraction sockets to heal during leveling and alignment before commencement of en-masse anterior retraction.

  • ProcedureLate Maxillary First Premolar Extraction

    Bilateral extraction of the maxillary first premolars will be performed after completion of leveling and alignment and one month of stabilization on a 0.019 × 0.025-inch stainless steel archwire, immediately before commencement of en-masse anterior retraction.

06

What researchers measure

Primary outcomes

  1. Rate of Orthodontic Space Closure Measured on Digital 3D Dental Models

    Intraoral scans will be obtained to generate digital 3D dental models at baseline (T0), 3 months (T1), and 6 months (T2) after initiation of en-masse anterior retraction. The extraction space will be measured in millimeters as the linear distance between the highest convexity on the mesial surface of the maxillary second premolar and the distal surface of the maxillary canine. The rate of space closure will be calculated as the reduction in extraction-space width over the corresponding observation period and expressed in millimeters per month (mm/month).

    Time frame: Baseline (T0), 3 months (T1), and 6 months (T2) after initiation of en-masse anterior retraction

Secondary outcomes

  1. Incidence and Severity of Gingival Clefts Assessed Clinically Using a Periodontal Probe

    Gingival clefts will be assessed clinically using a periodontal probe.The presence, severity (depth and width in mm), and type (buccal, lingual, or through-and-through) of gingival clefts will be recorded. Cleft severity will be assessed by measuring depth and width in millimeters. Depth will be measured perpendicular to the occlusal plane, and the width will be measured parallel to the occlusal plane from the buccal and lingual aspect, with the greater of the two measurements recorded as the cleft width.

    Time frame: Baseline (T0), 3 months (T1), and 6 months (T2) after initiation of en-masse anterior retraction

  2. Linear Mesial Movement of Maxillary First Molars Measured on Digital Models

    Measurements will be performed on digital dental models obtained by intraoral scanning. Linear mesial movement of the maxillary first molars will be measured in millimeters. Perpendicular reference lines to the mid-palatal suture will be constructed through the mesial contact point of the maxillary first molar and the medial end of the third palatal rugae. The distance between these reference lines will be measured in millimeters. The change in this distance from baseline (T0) to 3 months (T1) and from baseline to 6 months (T2) will represent linear mesial movement.

    Time frame: Baseline (T0), 3 months (T1), and 6 months (T2) after initiation of en-masse anterior retraction

  3. Ease of Maxillary First Premolar Extraction Assessed by Surgeon-Rated 4-Point Likert Scale and Extraction Duration

    Surgeon-perceived ease of extraction will be assessed using a 4-point Likert scale: 1 = very easy, 2 = easy, 3 = difficult, and 4 = very difficult, with higher scores indicating greater extraction difficulty. Extraction duration will also be recorded from the time the forceps are clamped onto the tooth until the tooth is completely removed from the socket.

    Time frame: Periprocedural

  4. Patient-Reported Pain and Dental Anxiety Associated With Premolar Extraction

    Pain will be assessed using a 0-10 Visual Analogue Scale, where 0 represents no pain and 10 represents the worst pain. Dental anxiety will be assessed using a 5-item questionnaire, with each item rated from 1 (not anxious) to 5 (extremely anxious), giving a total score of 5-25. Higher scores indicate greater pain or anxiety.

    Time frame: Dental anxiety immediately before extraction; pain immediately following extraction.

07

Study locations

1 of 1 sites recruiting
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Jul 2026 (actual). Primary completion is estimated for Jan 2028, 18 months after the start.

Of 23 interventional studies with no phase under Malocclusion, Angle Class I, half reached primary completion within 21 months of starting (the median), counting those still running; a quarter within 15 and three quarters within 24. This study's planned 18 months is below that.

How these figures are worked out, and which studies are left out of them.

Registered
Aug 12, 2026
First posted
Aug 19, 2026
StartActual
Jul 22, 2026
Primary completionEst.
Jan 2028
CompletionEst.
Jun 2028
Last update
Aug 19, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Aug 19, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07773389
Lead sponsor
Shifa College of Dentistry
Responsible party
Shanzay Khan (Postgraduate Resident in Orthodontics, Shifa College of Dentistry) — Principal investigator
First posted
Aug 19, 2026
Start date
Jul 22, 2026
Primary completion
Jan 2028 (estimated)
Completion
Jun 2028 (estimated)
Last update
Aug 19, 2026

Study contacts

Shanzay Khan, BDS, Post Graduate Resident
Contact
shanzaykhan1997@gmail.com
03245555716

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

Contact study team

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion