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Not yet recruitingNCT07935902Updated Nov 13, 2026

Effect of Different Adhesive Removal Techniques After Orthodontic Bracket Debonding on Postoperative Hypersensitivity: A Randomized Clinical Trial

An interventional study of Low-Speed Tungsten Carbide Bur and Fiberglass Bur in Dentin Sensitivity, Orthodontic Adhesive Removal and Postoperative Hypersensitivity, sponsored by Asmaa Badr Abdelfatah. Not yet recruiting at 1 site in Egypt. Open to participants aged 15 Years to 45 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-11-13.

Sponsored by Asmaa Badr Abdelfatah · Not applicable, Interventional, and Treatment

Updated Nov 13, 2026Newly registeredGo to Updates ↓

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Phase
Not applicable
Study type
Interventional
Enrollment
15
Allocation
Randomized
Ages
15 Years to 45 Years
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-13

Among 34 studies in Dentin Sensitivity with a site in Egypt — 7 open to participants now, 9 under way, 1 of them phase 3. Dentin Sensitivity · Egypt.

Planned enrollment
31st of 33
15 · median 48
Started
2026
with 2 others
No phase
25 of 34
6 open now
Registered
34th of 34
by date
Lead sponsor
1 of 34
Asmaa Badr Abdelfatah

Among the 34 studies in Dentin Sensitivity with a site in Egypt, this one is the 31st largest by planned enrollment of the 33 interventional ones that give a count, is one of 3 that started in 2026, is one of 25 with no phase, and was the 34th registered.

Dentin Sensitivity

288 studies on the registry are indexed under Dentin Sensitivity; 46 are open to participants now.

Browse Dentin Sensitivity studies →

Open to participants now

7 of the 34 studies in Dentin Sensitivity with a site in Egypt are open now. Recruiting first, the newest first:

1 more — sign in →

All 7 open studies →

A study can be open while its sites in Egypt have not opened yet or have stopped. Only those recruiting at a site in Egypt →

Who these studies take

Of the 18 Dentin Sensitivity studies recruiting now, 6 (33%) set no upper age limit and 11 (61%) stop at 75 or younger; 1 takes children under 18; 11 take healthy volunteers.

This study: 15 Years to 45 Years · all sexes · healthy volunteers too.

The full table on the hub →

This tab as a report to print or save as PDF → With an account.

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Watch this landscapeDownload CSVNarrow it in search →With an account: a weekly mail of what changed among 34 studies in Dentin Sensitivity with a site in Egypt, or all of them as a file.
02

Study summary

The objective of this randomized clinical trial is to evaluate and compare the effect of four different residual adhesive removal techniques following orthodontic bracket debonding on postoperative tooth hypersensitivity. The study compares low-speed tungsten carbide burs against fiberglass burs, white stone burs, and rubber-impregnated polishing points. Postoperative hypersensitivity will be evaluated using a Visual Analogue Scale (VAS) with an air-blast stimulus test immediately after debonding, at 24 hours, and at 7 days follow-up.

03

Conditions studied

  • Dentin Sensitivity
  • Orthodontic Adhesive Removal
  • Postoperative Hypersensitivity

Browse trials for

Keywords

  • Orthodontic Debonding
  • Fiberglass Bur
  • Postoperative Hypersensitivity
04

Who can participate

Ages eligible
15 Years to 45 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

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

  • Patients of any gender aged 15 to 45 years undergoing routine fixed labial orthodontic bracket removal across anterior and premolar teeth in both jaws.
  • Systemically healthy patients.
  • Good oral hygiene with a healthy, intact periodontium without clinical attachment loss or gingival recession.
  • Patients capable of reliably recording subjective discomfort on a Visual Analogue Scale (VAS) and willing to attend follow-up visits.
  • Sound fully erupted permanent incisors, canines, and premolars bonded with conventional stainless steel labial brackets.
  • Labial enamel surfaces free of visible pre-existing enamel defects, structural hypoplasia, severe fluorosis, or restorations.

Exclusion criteria

Exclusion Criteria:

  • Active use of systemic analgesics, NSAIDs, , or centrally acting pain medications within 14 days prior to debonding.
  • Use of desensitizing toothpastes, mouthwashes, or topical fluoride varnishes within 30 days prior to the trial.
  • Heavy bruxism, clenching habits, or pathological wear/erosion extending into dentin.
  • Pregnant or lactating female patients.
  • Teeth with irreversible pulpitis, pulpal necrosis, history of endodontic treatment, or periapical pathology.
  • Teeth with active carious lesions or exposed cervical dentin/cementum.
  • Teeth with severe, deep enamel microcracks identified at baseline examination.
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Corticosteroids (steroids)

Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.

Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
15 participants (estimated)

Study arms

  • Active comparator
    Active Comparator: Low-Speed Tungsten Carbide Bur

    Residual composite adhesive remnants on eligible teeth are cleaned using a 12-fluted low-speed tungsten carbide bur operated at 15,000-20,000 rpm under continuous water cooling.

    Device: Low-Speed Tungsten Carbide Bur

  • Experimental
    Fiberglass Bur

    Residual composite adhesive remnants on eligible teeth are cleaned using a fiberglass bur operated at 15,000-20,000 rpm under continuous water cooling

    Device: Fiberglass Bur

  • Experimental
    White Stone Bur

    Residual composite adhesive remnants on eligible teeth are cleaned using a fine-grit white stone bur (aluminum oxide) operated at 10,000-15,000 rpm under continuous water cooling.

    Device: White Stone Bur

  • Experimental
    Rubber-Impregnated Polishing Point

    Residual composite adhesive remnants on eligible teeth are cleaned using a rubber-impregnated polishing point operated at 10,000-15,000 rpm under continuous water cooling

    Device: Rubber-Impregnated Polishing Point

Interventions

  • DeviceLow-Speed Tungsten Carbide Bur

    Composite resin is removed using a 12-fluted tapered low-speed tungsten carbide bur operated at 15,000-20,000 rpm under continuous air-water spray irrigation until all visible adhesive remnant is completely eliminated.

  • DeviceFiberglass Bur

    Composite resin remnants are eliminated using a fiberglass resin-removal bur operated at 15,000-20,000 rpm under continuous air-water spray irrigation until all visible material is completely removed.

  • DeviceWhite Stone Bur

    Composite resin remnants are removed using a fine-grit Arkansas white stone bur (aluminum oxide) operated at 10,000-15,000 rpm under continuous air-water spray irrigation until the enamel surface is clear.

  • DeviceRubber-Impregnated Polishing Point

    Residual adhesive tags are removed and polished using a rubber-impregnated composite polishing point operated at 10,000-15,000 rpm under continuous air-water spray irrigation

06

What researchers measure

Primary outcomes

  1. Postoperative Hypersensitivity

    Patient-reported pain and hypersensitivity evaluated using a Visual Analogue Scale (VAS) score ranging from 0 (No pain) to 10 (Unbearable severe pain) in response to a 2-second dental syringe air-blast stimulus test.

    Time frame: Baseline (immediately post-debonding, before clean-up), 24 hours, and 7 days post-adhesive removal.

Secondary outcomes

  1. Procedure Time

    Time taken to perform complete residual adhesive removal per tooth, measured using a stopwatch

    Time frame: Immediately during the clean-up procedure.

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

1 registry update 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

Start is estimated for Nov 2026; primary completion for Jun 2027, 7 months later.

Of 111 non-industry interventional studies with no phase under Dentin Sensitivity, half reached primary completion within 7 months of starting (the median), counting those still running; a quarter within 4 and three quarters within 12. This study's planned 7 months is close to that.

Counting every sponsor, half of 144 studies reached it within 6 months; a quarter within 3 and three quarters within 10.

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

Registered
Nov 9, 2026
First posted
Nov 13, 2026
StartEst.
Nov 2026
Primary completionEst.
Jun 2027
CompletionEst.
Oct 2027
Last update
Nov 13, 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.
Registered
First appeared on the registry. No changes since
Nov 13, 2026
Show all 1 update
  1. Nov 13, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07935902
Lead sponsor
Asmaa Badr Abdelfatah
Responsible party
Asmaa Badr Abdelfatah (Assistant Lecturer, Master Candidate, Cairo University) — Sponsor-investigator
First posted
Nov 13, 2026
Start date
Nov 2026 (estimated)
Primary completion
Jun 2027 (estimated)
Completion
Oct 2027 (estimated)
Last update
Nov 13, 2026

Study contacts

Asmaa Badr Abdelfatah, BDS
Contact
asmaa.abdelfatah@dentistry.cu.edu.eg
+20 1148106593
Heba El-Deeb, PhD
Contact
heba.eldeeb@dentistry.cu.edu.eg
+20 106 610 9461
Heba El-Deeb, PhD
study director · Cairo to Department of Conservative Dentistry, Faculty of Dentistry, Cairo University .

Oversight

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

Not currently enrolling

This study is not yet recruiting, as verified in Nov 2026. You cannot join it, but the record below documents what was studied.

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Discussion

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