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Active, not recruitingNCT07907393Updated Oct 30, 2026

Comparison of Intraoperative Outcomes of Microdebrider-Assisted Versus Conventional Functional Endoscopic Sinus Surgery in Patients With Sinonasal Polyposis

An interventional study of Microdebrider-Assisted Functional Endoscopic Sinus Surgery and Conventional Functional Endoscopic Sinus Surgery in Nasal Polyps, sponsored by Lahore General Hospital. Active, not recruiting at 1 site in Pakistan. Open to participants aged 18 Years to 70 Years. Per ClinicalTrials.gov, last updated 2026-10-30.

Sponsored by Lahore General Hospital · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 4 months after the study started (first participant enrolled Jun 2026, registered Oct 2026).
Updated Oct 30, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
56
Allocation
Randomized
Ages
18 Years to 70 Years
Sex
All
01

Study summary

This study compared two surgical techniques for patients with nasal polyps affecting both sides of the nose and sinuses. Nasal polyps were soft swellings that caused symptoms such as nasal blockage, nasal discharge, and reduced sense of smell. The study assessed whether the amount of blood lost during surgery and the time required to complete surgery differed between microdebrider-assisted and conventional functional endoscopic sinus surgery.

The randomized controlled study was conducted in the Department of Ear, Nose and Throat at Lahore General Hospital, Lahore, over six months. It included 56 patients aged 18-70 years whose symptoms had persisted despite at least eight weeks of medical treatment. Patients were randomly assigned to two groups of 28 using sealed envelopes. Both groups underwent surgery under general anesthesia. In the microdebrider-assisted group, a powered instrument that cut and suctioned tissue simultaneously was used to remove the polyps. In the conventional group, standard surgical instruments, including forceps and curettes, were used.

Blood loss was measured in milliliters using the fluid collected through suction, after subtracting irrigation fluid, and the change in surgical sponge weights. Operative duration was recorded in minutes. These measurements were compared between the two groups. The study hypothesis was that microdebrider-assisted and conventional surgery differed in intraoperative blood loss and operative duration.

02

Conditions studied

  • Nasal Polyps

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Keywords

  • Bilateral sinonasal polyposis
  • Functional endoscopic sinus surgery
  • Microdebrider-assisted sinus surgery
  • Conventional endoscopic sinus surgery
  • Intraoperative blood loss
03

In context

Nasal Polyps

236 studies on the registry are indexed under Nasal Polyps; 68 are open to participants now.

This study's planned enrollment of 56 is close to the median of 60 across 181 interventional studies indexed under Nasal Polyps.

Browse Nasal Polyps studies →

Lead sponsor

Lahore General Hospital is the lead sponsor of 32 studies on the registry; 4 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 70 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

  • Adult patients aged 18-70 years diagnosed with bilateral sinonasal polyposis requiring surgical intervention.
  • Patients with persistent symptoms such as nasal obstruction, anosmia, or rhinorrhea despite at least 8 weeks of optimized medical management, including systemic and intranasal .
  • CT scan showing Lund-Mackay scores ≥8 on each side.

Exclusion criteria

Exclusion Criteria:

  • Patients with a history of previous sinus or nasal surgeries.
  • Cases with unilateral nasal polyposis or sinonasal tumors.
  • Patients with bleeding disorders, on antiplatelet therapy, or with active sinonasal infections.
  • Patients presenting with nasal polyposis secondary to fungal sinusitis, chronic granulomatous disease, or cystic fibrosis.
  • Pregnant or lactating women due to surgical and anesthetic risks.
  • Patients with 4-6.
  • Patients requiring simultaneous additional surgeries, such as septoplasty or turbinate reduction, to avoid confounding factors.
Terms in these criteria, in plain language(2)

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.

ASA physical status

The anaesthetists’ scale of health before surgery: I is healthy, II has a mild illness that is under control, III a severe one, IV a severe illness that is a constant threat to life. V and VI are used for the critically ill and for organ donors.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
56 participants (estimated)

Study arms

  • Experimental
    Group A-Microdebrider-Assisted Functional Endoscopic Sinus Surgery

    Patients underwent microdebrider-assisted functional endoscopic sinus surgery under general anesthesia following nasal decongestion with topical vasoconstrictors. Nasal polyps were removed using a microdebrider.

    Procedure: Microdebrider-Assisted Functional Endoscopic Sinus Surgery

  • Active comparator
    Group B-Conventional Functional Endoscopic Sinus Surgery

    Patients underwent conventional functional endoscopic sinus surgery under general anesthesia following nasal decongestion with topical vasoconstrictors. Nasal polyps were removed using conventional surgical instruments.

    Procedure: Conventional Functional Endoscopic Sinus Surgery

Interventions

  • ProcedureMicrodebrider-Assisted Functional Endoscopic Sinus Surgery

    A powered microdebrider was used under endoscopic guidance to cut and suction polyp tissue simultaneously.

  • ProcedureConventional Functional Endoscopic Sinus Surgery

    Polyp tissue was removed under endoscopic guidance using standard instruments, including forceps and curettes.

06

What researchers measure

Primary outcomes

  1. Mean Intraoperative Blood Loss

    ntraoperative blood loss was measured in milliliters by combining the blood volume collected in the suction container, after subtracting irrigation fluid, with blood loss estimated from the difference between surgical sponge weights before and after use. Mean blood loss was compared between the microdebrider-assisted and conventional surgery groups.

    Time frame: During the surgical procedure, with total blood loss assessed at the completion of surgery.

  2. Mean Operative Duration

    Operative duration was measured in minutes using a digital stopwatch, from the initial insertion of the endoscope until completion of surgery, including removal of all surgical instruments. Mean operative duration was compared between the microdebrider-assisted and conventional surgery groups.

    Time frame: From initial insertion of the endoscope to completion of surgery during the same operative session.

07

Study locations

1 site
08

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Jun 2026 (actual). Primary completion is estimated for Nov 2026, 5 months after the start.

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

Registered
Oct 25, 2026
First posted
Oct 30, 2026
StartActual
Jun 1, 2026
Primary completionEst.
Nov 1, 2026
CompletionEst.
Nov 1, 2026
Last update
Oct 30, 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
Oct 30, 2026
Show all 1 update
  1. Oct 30, 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 ↗

09

Registry details

Key details

Study ID
NCT07907393
Lead sponsor
Lahore General Hospital
Responsible party
Muhammad Irfan Jamil (Principal Investigator, Lahore General Hospital) — Principal investigator
First posted
Oct 30, 2026
Start date
Jun 1, 2026
Primary completion
Nov 1, 2026 (estimated)
Completion
Nov 1, 2026 (estimated)
Last update
Oct 30, 2026

Study contacts

Syed Mushahid Raza
principal investigator · Lahore General Hospital, Lahore

Oversight

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

Not currently enrolling

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

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