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Agitation and Pain relief in rinoseptoplasty surgeries

Effects of Oral Clonidine versus Pregabalin on smooth emergence from sevoflurane in adults undergoing rinoseptoplasty surgeries

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
PACTR
Registry ID
PACTR201709002556259
Enrollment
Unknown
Registered
2017-08-26
Start date
2017-09-10
Completion date
Unknown
Last updated
2026-09-14

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

Conditions

Ear, Nose and Throat Respiratory Surgery agitation and postoperative pain relief in rinoseptoplasty surgeries with sevoflurane anesthesia.

Interventions

oral clonidine group
oral pregabalin group
oral placebo group

Sponsors

Faculty of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: ASA physical status I and II patients, scheduled for nasal septoplastic surgeries

Exclusion criteria

Exclusion criteria: patients with history of cardiovascular, hepatic or renal disease, chronic pain, history of any kinds used of allergy to clonidine, Pregabalin or other drugs during general anesthesia, history of drug or alcohol abuse and taking clonidine or Pregabalin or ¿ blockers before the surgery except for the study protocol. Also, patients with psychiatric illness or on psychotropic medications are excluded from the study.

Design outcomes

Primary

MeasureTime frame
decreasing agitation postoperatively in patients undergoing rinoseptoplasty surgeries with sevoflurane anesthesia—

Secondary

MeasureTime frame
decreasing postoperative pain in patients undergoing rinoseptoplasty surgeries with sevoflurane anesthesia—

Countries

Egypt

Contacts

Public ContactSabry Abdallah

Lecturer of anesthesia and intensive Care, Faculty of Medicine, Menoufia University.

sabryabdallah222@yahoo.com00201012378888

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026