The comparison between administration of morphine and paracetamol for pain management in nose surgery

The comparison between administration of morphine and paracetamol before surgery and paracetamol after surgery for pain management in patients with septorhinoplasty

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT2014010615102N2

Enrollment

120

Registered

2014-02-11

Start date

2012-02-20

Completion date

Unknown

Last updated

2018-02-22

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

Conditions

pain management in septorhinoplasty. Acute Pain

Interventions

Intervention 1: group 1: patients who receive 1 gr of paracetamol IV in 30 minutes, 2 hours before induction of anesthesia. Intervention 2: group2: patients who receive 1 gr of paracetamol IV in 30 m

Treatment - Drugs

group 1: patients who receive 1 gr of paracetamol IV in 30 minutes, 2 hours before induction of anesthesia.

group2: patients who receive 1 gr of paracetamol IV in 30 minutes after surgery and in recovery.

group3: patients who receive 3 mg morphine IV in 1 min, after surgery and in recovery

Eligibility

Sex/Gender

All

Age

15 Years to 60 Years

Inclusion criteria

Inclusion criteria: inclusion criteria:patients who have septorhinoplasty surgery from February 2012 till March 2013; patients with 15-60 years-old; 24 hours admission at ENT ward after surgery; filling out the consent form for the trial. exclusion criteria: any history of psychiatric problem such as migraine, depression and psychosis;any history of drug abuse such as morphine and acetaminophen codeine; any complications during or after surgery such as hypoxia, hypercarbia and heart attack and arrest ; any complications after surgery such as infection, fever, bleeding from the site of surgery and inflammation symptoms; lack of patients' compliance during the trial; patients' will to leave the trial.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Pain. Timepoint: every 2 hour during the first 24 hours after surgey. Method of measurement: Asking the patient: based on the scale of 0-10 that was told to the patient before surgery.;The prescribed morphine within 24 hours after surgery. Timepoint: every 2 hour during the first 24 hours after surgey. Method of measurement: scale (Weighing the patient).;Nause and vomitting after surgery. Timepoint: every 2 hour during the first 24 hours after surgey. Method of measurement: Asking the patient: Presence or Absence.;Apnea. Timepoint: every 2 hour during the first 24 hours after surgey. Method of measurement: Examing the patient: Presence or Absence.	—

Measure

Time frame

Pain. Timepoint: every 2 hour during the first 24 hours after surgey. Method of measurement: Asking the patient: based on the scale of 0-10 that was told to the patient before surgery.;The prescribed morphine within 24 hours after surgery. Timepoint: every 2 hour during the first 24 hours after surgey. Method of measurement: scale (Weighing the patient).;Nause and vomitting after surgery. Timepoint: every 2 hour during the first 24 hours after surgey. Method of measurement: Asking the patient: Presence or Absence.;Apnea. Timepoint: every 2 hour during the first 24 hours after surgey. Method of measurement: Examing the patient: Presence or Absence.

—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactShahryar Omidvari

Shiraz University of Medical Sciences

omidvarish@yahoo.com+98 71 1626 2033

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026