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Efficacy of I/v Nalbuphine v/s Iv Lignocain in Attanuation of Pressor Responseduring Laryngeoscopy and Intubation in Middle Age Patient Planned for Thyroid Surgery

S

Sheikh Zayed Medical College

Status and phase

Not yet enrolling
Early Phase 1

Conditions

Hemodynamic Stability

Treatments

Drug: Lignocaine

Study type

Interventional

Funder types

Other

Identifiers

NCT05298761
ASarwar

Details and patient eligibility

About

Comparison of I/V nalbuphine versus I/V xylocain in attanuation of pressor response during intubation and laryngeoscopy in patients undergoing for thyroid surgery,selection of better supressor agent minimises the drug repated side effects like hypertention tachycardia but also helps in heamodynamically stability at induction.

Enrollment

60 estimated patients

Sex

All

Ages

18 to 40 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • middle age(18_40)
  • Asa 1 and 2
  • Non hypertensive
  • Thyroid patients
  • patient who gives consent

Exclusion criteria

  • hypertensive
  • Asa 3 and 4
  • Patient refusal

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

60 participants in 2 patient groups

Lignocain
Experimental group
Description:
I/V lignocain 1.5mg per kg given to participants in state dose
Treatment:
Drug: Lignocaine
nalbuphine
Experimental group
Description:
I/v nalbuphine 0.1mg per kg given to participants in stat dose
Treatment:
Drug: Lignocaine

Trial contacts and locations

1

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Central trial contact

Dr.amna Sarwar, Fcps

Data sourced from clinicaltrials.gov

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