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Subconjunctival Bupivacaine in Strabismus Surgery

F

Fayoum University

Status

Unknown

Conditions

Anesthesia, Local

Treatments

Drug: Iocal anaesthetic bupivacaine
Drug: Placebo

Study type

Interventional

Funder types

Other

Identifiers

NCT04782960
Subconjunctival bupivacaine

Details and patient eligibility

About

This study aimed to assess the effectiveness of the Subconjunctival bupivacaine on postoperative pain in Strabismus surgery under general anaesthesia.

Full description

40 patients will schedule for elective Strabismus surgery under general anaesthesia and randomly allocated into two groups to receive Subconjunctival 0.5%Bupivacaine group(B) or Subconjunctival placebo 0.9% normal saline group at the end of the surgery and assess the postoperative pain at 0th,30th, 60th,2nd h, 4h,6h,12h,24h.and post operative nausea and vomiting.

Enrollment

40 estimated patients

Sex

All

Ages

14 to 30 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • All patients aged 14 _30 years old with body mass index 18_28kg/m.
  • American Anaesthesiologist Association physical states I,II.
  • singed informed consent to participate in the study and were scheduled for strabismus operations under general anaesthesia.

Exclusion criteria

  • were patients with chronic pain.
  • ocular hypertension.
  • inability to communicate.
  • history of hematological disease.
  • allergy to local anesthetic drugs.

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

40 participants in 2 patient groups, including a placebo group

20 patients receive Subconjunctival bupivacaine of the end of the surgery
Active Comparator group
Description:
20 patients receive Subconjunctival bupivacaine in the end of operation and monitoring postoperative pain score
Treatment:
Drug: Iocal anaesthetic bupivacaine
20 patients receive Subconjunctival placebo in the end of operation
Placebo Comparator group
Description:
20 patients receive Subconjunctival placebo in the end of operation and monitoring postoperative pain score
Treatment:
Drug: Placebo

Trial contacts and locations

0

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Central trial contact

Abeer Sh Goda; Amr H Mahmoud, Msc

Data sourced from clinicaltrials.gov

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