Skip to content

The role of adding topical corticosteroids in anesthesia and analgesia after nasal surgery.

Comparison of local anaesthetic effect of Bupivacaine ( Marcaine ) VS Bupivacaine and Dexamethasone in Nasal Surgery in Imam hospital of Ahwaz.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201104256288N1
Enrollment
60
Registered
2011-09-04
Start date
2011-08-23
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

Condition 1: local anaesthesia. Condition 2: Closed reduction of nasal bone fracture. Condition 3: Septoplasty. Condition 4: Rhinoplasty. Condition 5: FESS(Functional endoscopic sinus surgery). Local anaesthetics Fracture of nasal bones Deviated nasal septum Acquired deformity of nose Chronic sinusitis,Nasal polyp

Interventions

Intervention 1: In the control group, injectable solution of Marcaine is used for nerve blocking(Incisive nerve (columellar area),bilateral Infraorbital nerves and Supratrochlear nerves) during surge
In the control group, injectable solution of Marcaine is used for nerve blocking(Incisive nerve (columellar area),bilateral Infraorbital nerves and Supratrochlear nerves) during surgery and immediate
In the intervention group, injectable solution of Marcaine + Dexamethasone is used for nerve blocking(Incisive nerve (columellar area),bilateral Infraorbital nerves and Supratrochlear nerves) during

Sponsors

Ahwaz Jundi shapour University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 40 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria: All patients who admtited for nasal sugery(closed reduction of nasal bone fracture(NBF), septoplasty, rhinoplasty, endoscopic sinus surgery (FESS) or a combination of them) and went under general anesthesia in Imam Khomeini Hospital in Ahwaz. Exclusion Criteria: 1- Not in the specified age range. 2- Having a history of major cardiovascular diseases, hypertension, cerebrovascular accidents, diabetes and eye problems. 3- Having a history of hypersensitivity to local anesthetic agents such as lidocaine or their preservative compounds. 4- Lack of satisfaction or cancellation to participate in the study. 5- Not undergoing general anesthesia for any reason.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
The amount of postoperative pain. Timepoint: 1,2,4,6,12,24 houres after surgery. Method of measurement: Visual Analog Scale(VAS).;The need for oral or injectable analgesic drugs. Timepoint: In the first 24 hours after surgery. Method of measurement: Frequency of use of acetaminophen 325mg (oral tablets) or pethidine 20mg(intravenous injection).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDoctor Mahmood Hekmat shoar

Ahwaz Jundi shapour University of Medical Sciences

dr.mhekmat@yahoo.com+98 61 1333 3477

Outcome results

None listed

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