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Aminophylline on Recovery in Functional Endoscopic Sinus Surgery Under Dexmedetomidine Hypotensive Anesthesia

T

Tanta University

Status

Completed

Conditions

Dexmedetomidine
Functional Endoscopic Sinus Surgery
Aminophylline

Treatments

Drug: normal saline
Drug: Aminophylline group

Study type

Interventional

Funder types

Other

Identifiers

NCT05738135
36264PR58/1/23

Details and patient eligibility

About

This study will be conducted to evaluate the effect of intravenous aminophylline on hemodynamics and recovery of patients receiving dexmedetomidine infusion during functional endoscopic sinus surgery.

Full description

Aminophylline is a nonselective adenosine receptor antagonist used for the treatment of asthma and chronic obstructive pulmonary disease. It has been used to antagonize the effects of anaesthetic and analgesic agents

Enrollment

52 patients

Sex

All

Ages

18 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Patients aged between 18 to 50 years, have American society of anesthesiology (ASA) physical status I - II and scheduled for elective FESS under general anesthesia and receiving dexmedetomidine infusion for controlled hypotension during surgery.

Exclusion criteria

  1. Patients with central nervous system diseases, cardiovascular diseases, hypertension, arrhythmias, cerebrovascular diseases, convulsions, renal impairment or hepatic dysfunction.
  2. Pregnancy or lactation.
  3. Patients with a history of allergy to aminophylline.
  4. Patients with recurrent sinus surgery, hypertension.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

52 participants in 2 patient groups, including a placebo group

Aminophylline group
Experimental group
Description:
Patients will receive 4 mg/kg aminophylline diluted in 50 ml normal saline over 30 minutes.
Treatment:
Drug: Aminophylline group
Control group
Placebo Comparator group
Description:
Patients will receive 50 ml normal saline over 30 minutes.
Treatment:
Drug: normal saline

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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