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A New Membrane Obturator Prothesis Concept for Soft Palate Defects

A New Membrane Obturator Prothesis Concept for Soft Palate Defects

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04009811
Acronym
VELOMEMBRANE
Enrollment
4
Registered
2019-07-05
Start date
2020-07-17
Completion date
2022-07-15
Last updated
2023-02-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Deglutition Disorders, Mouth Neoplasms, Speech Disorders, Velopharyngeal Insufficiency

Keywords

Randomized controlled trial, Palatal obturators

Brief summary

When soft palate defects lead to palatal insufficiency, the patient's quality of life is affected by difficulties swallowing, hypernasality, and poor intelligibility of speech. If immediate surgical reconstruction is not an option, the patient may benefit from the placement of a rigid obturator prosthesis. Unfortunately, the residual muscle stumps are often unable to adequately move this stiff and inert obturator to properly restore the velopharyngeal valve function. The objective of this case report was to describe the use of a membrane obturator prosthesis that incorporates a dental dam to compensate for the soft palate defect.

Detailed description

The velopharyngeal sphincter seals the oropharynx from the nasopharynx during swallowing and speech. This three-dimensional muscular valve closes through the synergistic behavior of the soft palate and the lateral and posterior walls of the pharynx. A soft palate defect surgically acquired in the context of oral cancer may impede complete closure and lead to a palatopharyngeal insufficiency. The resultant airflow escape results in hypernasality, poor speech intelligibility, and swallowing problems (such as leakage of foods and fluids into the nasal airways). The best way to rehabilitate and restore chewing and swallowing is one of the top ten research priorities in head and neck cancer. When the velopharyngeal function cannot be immediately restored with surgical reconstruction, patients can benefit from an obturator prosthesis. This obturator is a rigid extension of acrylic resin positioned at the level of the hard palate that provides surface contact for the remaining musculature. Often, the residual muscle stumps cannot move adequately around this stiff and inert obturator to properly restore the velopharyngeal valve function. The resulting blockage, or free space between the tissues and obturator, is a main cause of prosthetic failure. Subsequently, in many cases, oral functions remain impaired, with a negative impact on the patient's quality of life. The compensating treatment consists of a provisional removable partial denture (RPD) with a membrane obturator. The membrane consisted of a thick dental dam shaped with scissors to create a 10-mm overlap with the pharyngeal walls that was then perforated with four holes using punch pliers. The follow-up ends after the last visit. However, our team can provide cares of any patient seeking for dental care, prosthetic treatments and routine follow-up.

Interventions

DEVICESuersen and membraneous obturators evaluation

The patient will wear one month each obturator prothesis (Suersen and membraneous obturators). The order of evaluation will be randomized in two arms. Half of patient will first wear one month the membranous obturator then one month the Suersen, the other half of patient will first wear one month the Suersen obturator and one month the membranous obturator.

Sponsors

University Hospital, Bordeaux
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adult over 18 year-old * Acquired loss of velar or palato-velar substance (maxillectomies of Class I and II a-d, Brown 2010) following the excision of a tumor * Indication of Suersen obturator prosthesis rehabilitation * Possible dental rehabilitation with removable prosthesis (retention and stability prosthetic provided without the use of glue, mouth opening allowing fingerprints, presence of saliva, dexterity allowing the insertion and removal of prostheses, as well as the cleaning of devices) * Having given their consent to participate in the study * Speaking French, knowing how to read it * Available and motivated for regular follow-up during the study period

Exclusion criteria

* Child under 18 * Allergy to acrylic resin * Radiotherapy or chemotherapy in progress * Surgery of the veil programmed during the 3 months necessary for the realization and the wearing of the prostheses. * Loss of congenital or traumatic palato-velar substance * Maxillectomies including orbital floor or total maxillectomy * Pregnant or lactating woman * Participation in another interventional study * Inability to give informed consent

Design outcomes

Primary

MeasureTime frameDescription
Voice Handicap Index (VHI) overall scoreVisit M2 : one month after first obturator supply i.e. two months after inclusionMin : 0 = Non handicap to Max : 120 = voice handicap maximum

Secondary

MeasureTime frameDescription
Deglutition Handicap Index (DHI) overall scoreVisit M1 : one month after inclusionMin : 0 = Non handicap to Max : 120 = deglutition handicap maximum
Health-related quality of life EORTC QLQ-C30 questionnaire scoreVisit M1 : one month after inclusionMin : 0 = lower level of quality of life to Max : 100 = better level of quality of life
Head and Neck quality of life EORTC QLQ-H&N35 questionnaire scoreVisit M1 : one month after inclusionMin : 0 = lower level of quality of life to Max : 100 = better level of quality of life

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 18, 2026