Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02682134
Other study ID # AAlJabari
Secondary ID
Status Completed
Phase Phase 4
First received February 5, 2016
Last updated February 10, 2016
Start date November 2015
Est. completion date February 2016

Study information

Verified date February 2016
Source University of Jordan
Contact n/a
Is FDA regulated No
Health authority Jordan: Ethical Committee
Study type Interventional

Clinical Trial Summary

The aim of this interventional study is to find out the incidence of sore throat among intubated patients in Jordan university hospital and to find out which is preventive and effective method to decrease sore throat;is it xylocaine gel on endotracheal cuff as lubricant versus dexamethasone 8 mg intravenously or both.


Description:

Three groups were divided into: first group received xylocaine gel as endotracheal cuff lubricant,second group received dexamethasone 8 mg intravenously and third group received both( xylocaine and dexamethasone).

The investigator compared between the three groups regarding sore throat in intubated patients and followed them up to 48 hours.


Recruitment information / eligibility

Status Completed
Enrollment 300
Est. completion date February 2016
Est. primary completion date February 2016
Accepts healthy volunteers No
Gender Both
Age group 15 Years to 70 Years
Eligibility Inclusion Criteria:

- ASA 1-3.

- Elective VS Emergency.

- Cuffed endo-tracheal tubes.

- Different types of surgery.

Exclusion Criteria:

- Pregnant ladies.

- ICU patients.

- <15 years of age

- Laryngeal mask airway

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Single Blind (Subject), Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Drug:
xylocaine
First group were given xylocaine
Dexamethasone
Second group were given Dexamethasone
Xylocaine and Dexamethasone
Third group were given both Xylocaine and Dexamethasone

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University of Jordan

Outcome

Type Measure Description Time frame Safety issue
Primary Comparison in preventing sore throat: xylocaine gel versus dexamethasone or both following intubation. Questionnaire follow up in intubated patients. 4 months Yes
Secondary Sore throat SCALE Sore throat scale from None,mild,moderate till severe. 4 months Yes
See also
  Status Clinical Trial Phase
Recruiting NCT04083417 - Sore Throat in Primary Care - a Comparison of Phenoxymethylpenicillin and no Antibiotic Treatment Phase 4
Not yet recruiting NCT03517215 - The Development and Testing of a Scaling Strategy for a Community-Based Primary Care Antimicrobial Stewardship Program N/A
Not yet recruiting NCT01782183 - Thermographic Characteristics of Sore Throat by Thermographic Camera N/A
Completed NCT02608788 - S.L. Spray Solution® and Difflam® and Acular®Spray for the Prevention of Postoperative Sore Throat Phase 4
Completed NCT01986361 - Placebo-Controlled Onset-of-Action Study of Flurbiprofen Utilizing the Double-Stopwatch Method Phase 3
Completed NCT01118533 - Impact of Blades Used for Scheduled Orotracheal Intubation on Postoperative Sore Throat N/A
Completed NCT03397797 - Effect of Intraoperative Neuromuscular Blockade on Postoperative Sore Throat and Hoarseness
Completed NCT03282045 - Efficacy and Safety of the Lysobact Complete Spray®, Tantum Verde® and Pharyngal® Oromucosal Spray in the Treatment of Acute Sore Throat Phase 3
Completed NCT01902641 - Muscle Relaxation for Short Procedures N/A
Completed NCT01444703 - Comparison of Licorice Versus Sugar-water Gargle for Prevention of Postoperative Sore Throat and Postextubation Coughing N/A
Completed NCT00957996 - Safety Study of IV Peramivir in Hospitalized Subjects With Confirmed or Suspected Influenza Phase 3
Completed NCT01033799 - Effect of the Consumption of a Fermented Milk on Common Infections in Shift-workers N/A
Completed NCT05069844 - Preoperative Gum Chewing for Different Durations to Prevent Sore Throat After Endotracheal Intubation N/A
Completed NCT05247333 - Implementation of a Minor Ailment Service in Community Pharmacy Practice N/A
Recruiting NCT03369132 - Efficacy of Natural Seawater Based Throat Spray in Acute Sore Throat Relief N/A
Terminated NCT00958776 - A Study to Evaluate the Efficacy and Safety of IV Peramivir in Addition to Standard of Care Compared to Standard of Care Alone in Adults and Adolescents Who Are Hospitalized Due to Influenza Phase 3
Completed NCT00242281 - APC-111 MP Tablet Once a Day vs.Penicillin VK Four Times a Day Both for 10 Days in Patients With Strep Throat Phase 3
Completed NCT03729973 - Comparing Efficacy Preoperative Nebulized: Ketamine , Mgspo4 ,and Lidocaine In Attenuating Endotracheal Sore Throat Phase 3
Completed NCT04085744 - A Comparison Of Local Anesthetic Agents And Steroid On Tracheal Tube Cuff N/A
Completed NCT01506583 - Clinical Evaluation of QFlu Combo Test