Effect of using lidocaine spray 10% on satisfaction of patients under spinal anesthesia.

Evaluation of use of lidocaine spray 10% on satisfaction of patients under spinal anesthesia.

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20130120012203N11

Enrollment

200

Registered

2020-01-21

Start date

2017-04-04

Completion date

Unknown

Last updated

2020-02-24

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

Conditions

pain. Other acute post procedural pain

Interventions

Intervention 1: Intervention group: The lidocaine spray 10% is scattered 5 minutes before the spinal anesthesia is implemented at the injection site. Intervention 2: Control group: spry normal saline

Eligibility

Sex/Gender

All

Age

18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Indication of spinal anesthesia ASA Class 1: A normal healthy patient Addiction to opium

Exclusion criteria

Exclusion criteria: Skin lesions at the needle insertion site Patient dissatisfaction emergency surgeries

Design outcomes

Primary

Measure	Time frame
Acute pain. Timepoint: At the end of surgery. Method of measurement: Visual Analogue Scale (VAS).	—

Secondary

Measure	Time frame
Anxiety. Timepoint: At the end of surgery. Method of measurement: Anxiety with Zank questionnaire.;Cooperation. Timepoint: At the end of surgery. Method of measurement: The rate of cooperation with the questionnaire.;Satisfaction. Timepoint: At the end of surgery. Method of measurement: Using the questionnaire.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNilofar Massoudi

Shahid Beheshti University of Medical Sciences

massodi@sbmu.ac.ir+98 21 2207 4087

Outcome results

None listed

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