Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00773994
Other study ID # 07100381
Secondary ID
Status Completed
Phase N/A
First received October 15, 2008
Last updated October 17, 2017
Start date May 2008
Est. completion date July 15, 2015

Study information

Verified date October 2017
Source University of Pittsburgh
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This prospective research study seeks to determine how the normal velopharyngeal mechanism compares, both anatomically and physiologically, with previous data obtained on subjects with submucous cleft palate (SMCP) in IRB#07080395.


Description:

Televex videofluoroscopy utilizes real-time, x-ray imaging to visualize the velopharyngeal port from multiple views or planes. The views generally utilized include the lateral, base and frontal. This technique requires the subject to provide specific speech patterns, as presented by a speech pathologist, while a radiologist obtains adequate views of the velopharyngeal (VP) port. Each procedure will take about 3 to 5 minutes. Fluoroscopic imaging is provided only during speech tasks and swallowing limiting radiation exposure.

1) The radiologist begins by taking a lateral view while speaking, which allows viewing of the velum and posterior pharyngeal wall during speech production, as well as evaluation of cranial base angle, size and location of adenoid tissue, velar length, velar thickness and velar stretch. 2) The speech pathologist gives the subject barium sulfate contrast, approximately 2 to 4 oz, to swallow, which allows for better structure delineation, as well as the confirmation of the presence of palatal fistulae if barium passes through the palate during swallowing. 3) The speech pathologist places the subject in a supine position and barium sulfate is then instilled into the nasal passages bilaterally via syringe, approximately 5 ml. approximately 2. 5 ml in each nostril. This allows for nasopharyngeal coating of structures. 4) The speech pathologist then places the subject in the prone on the table and positioned into a sphinx position with head and neck extended and forearms and palms flat on the fluoroscopic table. The head, shoulders and neck are positioned to find the base view of the velopharyngeal port. This view affords the ability to obtain velopharyngeal closure patterns and size of velopharyngeal defect similar to that of nasopharyngoscopy. 5) The next view obtained by the radiologist is the frontal or anterior-posterior. This is obtained with the head/neck extended to allow for evaluation of the degree of lateral pharyngeal wall motion. 6) The final view obtained by the radiologist is a repeat of the initial lateral view this time with the nasopharyngeal coating in place. This can be beneficial in confirming VPI in the presence of a small VP gap. During the coated lateral view blowing of barium through the VP port can be observed. Additionally if barium is not dissipated during velopharyngeal closure this can be indicative of anatomic VPI. This is all done in the radiology department and takes approximately 3 minutes to 5 minutes.


Recruitment information / eligibility

Status Completed
Enrollment 4
Est. completion date July 15, 2015
Est. primary completion date July 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- All subjects for this study are adults.

- In this study, the most significant risk is that of radiation exposure, which for Televex videofluoroscopy, is comparable to a single undergoing a single x-ray study, and is significantly less than most CT scans.

- There are no risks to a fetus or pregnant subject involved in this study, nor are there any interventions involved in the research that may be associated with reproductive risks, because all female participants will be given a urine pregnancy test prior to undergoing the Televex Videofluoroscopy.

- All participants will wear protective lead torso and pelvic shields, which are standard for all personnel in a room where a radiologic evaluation is being performed.

Exclusion Criteria:

- The subjects for this study are all adult.

- None of the participants will be children because we are looking for subjects who have reached skeletal maturity which happens around the age of 18 years old

- Any positive urine pregnancy test results would exclude the female subject from this study.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Normal Velopharyngeal Mechansim
The amount of radiation exposure that you will receive from this procedure is about 0.3 rem to the head and neck, with minimal exposure of the other body areas.

Locations

Country Name City State
United States Children's Hospital of Pittsburgh of UPMC Pittsburgh Pennsylvania

Sponsors (1)

Lead Sponsor Collaborator
University of Pittsburgh

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Normalnormal velopharyngeal mechanism vs abnormal 2 years or 10 subjects.
See also
  Status Clinical Trial Phase
Completed NCT00340977 - Svangerskap, Arv, Og Miljo (Pregnancy, Heredity and Environment)
Completed NCT05166408 - Fistiulation Rate Following Primary Cleft Repair≤ N/A
Recruiting NCT03839290 - Development of the Palate in Bilateral Orofacial Cleft Newborns One Year After Early Neonatal Cheiloplasty
Recruiting NCT01867632 - Acellular Dermal Matrix in Primary Furlow Palatoplasty N/A
Completed NCT02900014 - Validation of a Production Method of Stem Cell Isolated From the Nasal Cavity for an Innovative Cell Therapy of Cleft Palate N/A
Withdrawn NCT02953145 - The Use of Fibrin Sealant to Reduce Post Operative Pain in Cleft Palate Surgery Phase 4
Completed NCT04725370 - Characterization of Cleft Lip and Palate Conditions in Guatemala
Withdrawn NCT03572907 - Use of Titanium Plate in Rhinoplasty in Patients With Cleft Lip and Palate : Aesthetic and Functional Impact.
Enrolling by invitation NCT02702869 - Allied Cleft & Craniofacial Quality-Improvement and Research Network (ACCQUIREnet)
Completed NCT02583100 - Improving Outcomes in Cleft Palate Surgery N/A
Recruiting NCT06072495 - Etiological Study of Persistent Velopharyngeal Insufficiency in Children With Operated Velopalatine Cleft by Analysis of Velopharyngeal Motor Skills in Static and Dynamic MRI N/A
Completed NCT04718558 - Optic Nerve Sheath Diameter Measurement in Cleft Palate Repair
Not yet recruiting NCT05357092 - Effects of AlignBabyCleft (ABaCleft) N/A
Completed NCT01500109 - Efficacy of Oral Versus Intravenous Acetaminophen for Primary Pediatric Cleft Palate Repair N/A
Completed NCT01252264 - FaceBase Biorepository
Completed NCT00397917 - Oral Cleft Prevention Program Phase 3
Enrolling by invitation NCT03632044 - Evaluation of Trigeminal Nerve Blockade Phase 4
Completed NCT04277273 - Characteristics of a Maxillofacial Prosthesis Consultation Within Assistance Publique - Hopitaux de Paris N/A
Completed NCT05405738 - Cleft Palate Technique and Maxillary Growth
Completed NCT03170505 - Using of Acellular Dermal Matrix in Cleft Palatal Fistula and Compare With Use of Conchal Cartolage N/A