Enhanced Recovery After Uvulopalatoplasty

NCT ID: NCT07246694

Last Updated: 2025-12-05

Study Results

Results pending

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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Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

80 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-12-31

Study Completion Date

2026-12-31

Brief Summary

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Obstructive sleep apnea is a prevalent condition often treated surgically with palatoplasty, which improves airway patency and reduces apneic events. However, postoperative pain and airway discomfort following palatoplasty can be significant, leading to delayed oral intake, increased opioid consumption, and prolonged recovery. Combining an ultrasound-guided glossopharyngeal nerve block with topical airway anesthesia may provide synergistic analgesia and support a safer recovery profile.

Detailed Description

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Obstructive sleep apnea is a prevalent condition often treated surgically with palatoplasty, which improves airway patency and reduces apneic events. However, postoperative pain and airway discomfort following palatoplasty can be significant, leading to delayed oral intake, increased opioid consumption, and prolonged recovery. Enhanced Recovery After Surgery protocols aim to accelerate functional recovery and reduce perioperative morbidity. Combining an ultrasound-guided glossopharyngeal nerve block with topical airway anesthesia may provide effective analgesia and support a smoother recovery profile.

Conditions

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Analgesia Recovery, Psychological

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Outcome Assessors

Study Groups

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Group I

The patient will receive the ultrasound-guided glossopharyngeal nerve block combined with topical airway anesthesia.

Group Type ACTIVE_COMPARATOR

Glossopharyngeal nerve block

Intervention Type PROCEDURE

Glossopharyngeal nerve block using ultrasound guidance after induction of general anesthesia plus topical anesthesia before surgical incision.

Group c

The patient will receive the standard multimodal analgesia.

Group Type ACTIVE_COMPARATOR

Standard multimodal analgesia

Intervention Type OTHER

The patient will receive intravenous fentanyl and non opioids analgesics (acetaminophen and non-steroidal anti-inflammatory drugs) with general anesthesia.

Interventions

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Glossopharyngeal nerve block

Glossopharyngeal nerve block using ultrasound guidance after induction of general anesthesia plus topical anesthesia before surgical incision.

Intervention Type PROCEDURE

Standard multimodal analgesia

The patient will receive intravenous fentanyl and non opioids analgesics (acetaminophen and non-steroidal anti-inflammatory drugs) with general anesthesia.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Confirmed diagnosis of moderate to severe obstructive sleep apnea.
* Patients scheduled for elective palatoplasty under general anesthesia.
* American Society of Anesthesiologists Physical Status class I and II.

Exclusion Criteria

* Patients with chronic opioid use.
* Advanced hepatic, renal, cardiovascular, and neurologic diseases.
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Zagazig University

OTHER_GOV

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Fatma Mahmoud Ahmed, MD

Role: PRINCIPAL_INVESTIGATOR

Department of Anesthesia, Intensive Care & Pain Management, Zagazig University

Alshaimaa Abdelfattah Kamel, MD

Role: STUDY_DIRECTOR

Department of Anesthesia, Intensive Care & Pain Management, Zagazig University

Osama Yehia Khalifa, MD

Role: STUDY_DIRECTOR

Department of Anesthesia, Intensive Care & Pain Management, Zagazig University

Locations

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Zagazig university hospital

Zagazig, Al-Sharkia, Egypt

Site Status

Countries

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Egypt

Central Contacts

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Mohamed

Role: CONTACT

011118851696

Osama Yehia, MD

Role: CONTACT

01007579438

Facility Contacts

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Mohamed Gaber, MD

Role: primary

01118851696

Other Identifiers

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Uvulopalatoplasty Analgesia

Identifier Type: -

Identifier Source: org_study_id

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