A Novel Approach for VC Lateralization, With Prolene Suture Stabilized Over Prolene Mesh
NCT ID: NCT05285423
Last Updated: 2022-09-28
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
39 participants
INTERVENTIONAL
2022-01-01
2022-07-01
Brief Summary
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Detailed Description
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Objective: To evaluate a new approach of vocal cord Lateralization using prolene suture and mesh.
Study Design: Interventional, prospective study. Place and Duration of study: Ent departments of multiple tertiary care hospitals of Pakistan from Jan 2022 to May 2022.
Materials and Methods: Hospital ethical committee's approval will be obtained. Patients of age 15 years onwards, with bilateral vocal cord paralysis/ paresis due to trauma and idiopathic causes will be included. Patients with neoplasm and underlying muscular dystrophy are to be excluded from the study. All patients will be counseled properly and given the choice of intervention by prolene Suture technique. Consenting patients will be subjected to routine blood investigations, fiber optic laryngoscopy, and imaging with a Computerized Tomography scan (where applicable). The surgery will be performed under General anesthesia. Tracheostomy is preferred to get an adequate view of the glottis and to ascertain the extent of lateralization intraoperatively. The incision will be made at the lower border of thyroid cartilage under aseptic measures. Skin flaps will be raised in the sub-platysmal plane, strap muscles will be separated in the midline to expose the laryngeal cartilaginous framework. Two wide bore Canula (16G) are passed at the levels just above and below the true Vocal cord under laryngoscopic guidance. Prolene 1-0 suture (thickness 0.3-0.4mm) thread is passed through the lower cannula and the thread end is brought out through the upper cannula bore under microscopic forceps guidance. Both the ends are now tied over the thyroid lamina with a prolene mesh between the knot and the cartilage. the tension of the knot determines the extent of lateralization needed. Wound will be closed in layers. The patient will be kept in hospital for a day or more for observation. The success of the surgical procedure will be measured in terms of post-operative decannulation of tracheostomy and preservation of reasonable postop voice with comfortable breathing altogether. Tracheostomy decannulation will be done between 24 to 48 hours post operatively. Preoperatively Voice and breathing parameters will be noted and Post operatively evaluated at day 14. For subjective evaluation of ease of breathing, pre and postoperative Visual Analog score (VASb) will be recorded at Rest and light exercise, graded from 1-10 (1 being the comfortable easy breathing and 10 being the most difficult). Peak expiratory flow (PEF) will be measured for an objective assessment of ease in breathing both pre and post operatively. For subjective assessment of voice quality, Visual analog score (VASV) (1-10) will be used both pre and postoperatively. It will be graded as 1 being the best voice and 10 the worse. For an objective assessment of the patient's voice, a customized Voice Handicap Index (VHI-10) will be used.
Modified VHI-10 Questionnaire:
My voice makes it difficult for people to hear me. 0 1 2 3 4 5
I run out of air when I talk. 0 1 2 3 4 5
People have difficulty understanding me in a noisy room. 0 1 2 3 4 5
I use a great deal of effort to speak. 0 1 2 3 4 5
My family has difficulty hearing me when I call them throughout the house. 0 1 2 3 4 5
I use my phone less often than I would like to. 0 1 2 3 4 5
I am tense when I am talking to others because of my voice. 0 1 2 3 4 5
I tend to avoid groups of people because of my voice. 0 1 2 3 4 5
People seem irritated with my voice. 0 1 2 3 4 5
People ask what's wrong with my voice. 0 1 2 3 4 5
VHI : Voice Handicap Index 0 = never, 1 = almost never (occasionally), 2 = sometimes, 3 = almost always, 4 = always
Modified Voice Handicap Index (VHI-10)
Routine monthly follow-up for 3 months will be advised after that.
The results will be analyzed using International IBM SPSS Statistics version 20. Variables defined would be compared between the preoperative and postoperative groups. For normal data paired sample t-test would be used and for abnormally distributed data nonparametric t-test would be used. A P-value of less than 0.05 will be taken as significant.
Conditions
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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Prolene suture technique.
The Group of Patients who were offered Vocal Cord Lateralization with prolene suture technique.
Novel technique of Vocal cord Laterlization with Prolene suture.
The procedure will be performed under General anesthesia, preferably with a tracheostomy so that the extent of vocal cord lateralization could be ascertained intraoperatively.
Interventions
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Novel technique of Vocal cord Laterlization with Prolene suture.
The procedure will be performed under General anesthesia, preferably with a tracheostomy so that the extent of vocal cord lateralization could be ascertained intraoperatively.
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
15 Years
100 Years
ALL
Yes
Sponsors
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Pak Emirates Military Hospital
OTHER
Responsible Party
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Muhammad Rashid
Muhammad Rashid, Head of The Department Otolaryngology, Kharian, The Principal Investigator.
Principal Investigators
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Muhammad N Karim, FCPS
Role: PRINCIPAL_INVESTIGATOR
CMH Sialkot
Locations
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ENT Departments
Sialkot, Punjab Province, Pakistan
Countries
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Other Identifiers
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Prolene VC Lateralization
Identifier Type: -
Identifier Source: org_study_id
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