Endoscopic Classic Versus Reversal Stapedotomy

Sponsor
Mansoura University (Other)
Overall Status
Completed
CT.gov ID
NCT05554796
Collaborator
(none)
60
1
2
13
4.6

Study Details

Study Description

Brief Summary

Aim of The Work The aim of this study is to compare hearing outcome and surgical complications between classic and reversal endoscopic stapedotomy.

Patients and Methods

Study design:

This study is a randomized clinical study and will be carried out at Otorhinolaryngology department at Mansoura University Hospitals. The study will be conducted among 60 patients with otosclerosis who will undergo endoscopic stapedotomy. The patients will be divided into two groups. The first group (group 1) 30 patients will undergo endoscopic classic stapedotomy while the second group (group 2) 30 patients will undergo endoscopic reversal stapedotomy.

The two groups will compared to each other as regard, A. Intra-operative time (in minutes) B. Hearing outcome. C. Surgical complications

Condition or Disease Intervention/Treatment Phase
  • Procedure: Endoscopic classic stapedotomy
  • Procedure: Endoscopic reversal stapedotomy
N/A

Detailed Description

Aim of The Work The aim of this study is to compare hearing outcome and surgical complications between classic and reversal endoscopic stapedotomy.

Patients and Methods

Study design:

This study is a randomized clinical study and will be carried out at Otorhinolaryngology department at Mansoura University Hospitals. The study will be conducted among 60 patients with otosclerosis who will undergo endoscopic stapedotomy. The patients will be divided into two groups. The first group (group 1) 30 patients will undergo endoscopic classic stapedotomy while the second group (group 2) 30 patients will undergo endoscopic reversal stapedotomy.

Inclusion criteria:

Patients with history of gradual progressive hearing loss with normal otoscopy. No history of ear discharge. No history of ipsilateral ear surgery. Air bone gap >20 dB with lost stapedial reflex

Exclusion criteria:

Cases who did not meet the inclusion criteria. Revision cases. Cases that lost to follow up. All cases with narrow oval window niche or obliterated footplate, because those are the contraindications of reversal technique as described by Fisch (Fisch et al., 1994).

The two groups will compared to each other as regard,

A. Intra-operative time (in minutes):

Starting from the incision till repositioning of the flap. B. Hearing outcome. Hearing outcomes will include the average air conduction pure-tone threshold (in dB HL) and a word recognition score (WRS, in %). The data will be reported on a scattergram relating average air conduction pure-tone threshold to the WRS.

Preoperative and postoperative air conduction (AC) and bone conduction (BC) thresholds will be recorded at frequencies of 0.5, 1, 2, and 3 khz. The air-bone gap (ABG) will be recorded as the difference between AC and BC thresholds. Postoperative air bone gap will be graded as grade A (0-10 dB), grade B (11-20 dB), grade C (21-30 dB) and grade D (>30 dB).

C. Surgical complications:

Vertigo. Incus subluxation. Corda tympani nerve injury. Tympanic membrane tear. Perilymph gusher. Floating footplate. Postoperative pain. Perilymph fistula. Immediate or late sensory neural hearing loss.

Method:
All cases planned to be included in this study will be subjected to:
History taking:

Personal history, past history of medical diseases, past history of surgery and family history.

Examination: routine ENT examination to exclude any other ear disease.

Investigations:
  1. PTA ,Tympanogram. B. Lab investigations: Pre-operative full lab(CBC, INR, LFT,virology)
Surgeries:

Patients will be operated under local anesthesia, and the transcanal approach will be the standard approach in both groups. Zero and thirty degree, 4 mm diameter, 18 cm length endoscopes and camera will be used.

Group 1:

Patients in this group will undergo classic stapedotomy where removal of stapes superstructure will be performed in the beginning followed by perforation of footplate and finally insertion of the Teflon piston.

Group 2:

Patients in this group will undergo reversal stapedotomy where perforation of footplate and insertion of Teflon piston will be done at the beginning followed by removal of stapes superstructure.

Statistical analysis:- Data analysis will be carried out using statistical software program (SPSS for Windows, version 28, USA). Variables will be presented as mean ± standard deviations (SDs), and percentages. The preoperative and postoperative hearing results (AC and BC and ABG) will be compared utilizing the paired t-test. Statistical significance will be considered at P <0.05.

Study Design

Study Type:
Interventional
Actual Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Endoscopic Stapedotomy: Classic Versus Reversal Technique
Actual Study Start Date :
Sep 1, 2021
Actual Primary Completion Date :
Sep 1, 2022
Actual Study Completion Date :
Oct 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Endoscopic classic stapedotomy

This groups contains 30 patients and will undergo classic stapedotomy

Procedure: Endoscopic classic stapedotomy
Patients in this group will undergo classic stapedotomy starting with removal of stapes superstructure then perforation of footplate and finally insertion of the Teflon piston.

Experimental: Endoscopic reversal stapedotomy

This groups contains 30 patients and will undergo reversal stapedotomy

Procedure: Endoscopic reversal stapedotomy
Patients in this group will undergo reversal stapedotomy where perforation of footplate and insertion of Teflon piston will be done at the beginning followed by removal of stapes superstructure.

Outcome Measures

Primary Outcome Measures

  1. Average air conduction pure-tone threshold [3 months]

    The average air conduction pure-tone threshold (in dB HL) will be calculated from pure-tone audiometry and presented in decibels (dB)

  2. Word recognition score [3 months]

    The word recognition score will be calculated from the the speech audiometry and presented as percentage (%)

  3. Average air bone gap [3 months]

    Preoperative and postoperative air conduction (AC) and bone conduction (BC) thresholds will be recorded at frequencies of 0.5, 1, 2, and 3 khz. The air-bone gap (ABG) will be recorded as the difference between AC and BC thresholds. Postoperative air bone gap will be graded as grade A (0-10 dB), grade B (11-20 dB), grade C (21-30 dB) and grade D (>30 dB).

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients with history of gradual progressive hearing loss with normal otoscopy.

  • No history of ear discharge.

  • No history of ipsilateral ear surgery.

  • Air bone gap >20 dB with lost stapedial reflex

Exclusion Criteria:
  • Cases who did not meet the inclusion criteria.

  • Revision cases.

  • Cases that lost to follow up.

  • All cases with narrow oval window niche or obliterated footplate, because those are the contraindications of reversal technique as described by Fisch (Fisch et al., 1994).

Contacts and Locations

Locations

Site City State Country Postal Code
1 Mansoura University Hospitals Mansoura Dakahlia Governorate Egypt 35511

Sponsors and Collaborators

  • Mansoura University

Investigators

  • Principal Investigator: Ahmed Hemdan, MD, Lecturer of Otorhinolaryngology

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Ahmed Hemdan, Lecturer of Otorhinolaryngology, Mansoura University
ClinicalTrials.gov Identifier:
NCT05554796
Other Study ID Numbers:
  • MS.21.11.1758
First Posted:
Sep 26, 2022
Last Update Posted:
Oct 31, 2022
Last Verified:
Oct 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 31, 2022