Incidence of transient neurologic symptom following intrathecal anesthesia with lidocaine in cesarean and factors affecting it.

Incidence of transient neurologic symptom (TNS) following intrathecal anesthesia with lidocaine in cesarean and factors affecting it.

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT201404211616N4

Enrollment

Registered

2014-05-15

Start date

2014-06-01

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

Transient neuorologic syndrom. Other transient cerebral ischaemic attacks and related syndromes

Interventions

Intervention 1: 25 g sprotte needle. Bupivacaine 25 g quincke needle. Bupivacaine. Intervention 2: 25 G sporotte needle, Lidocaine 25 G quincke needle, Lidocaine.

Treatment - Devices

25 g sprotte needle. Bupivacaine 25 g quincke needle. Bupivacaine

25 G sporotte needle, Lidocaine 25 G quincke needle, Lidocaine

Eligibility

Sex/Gender

Female

Age

20 Years to 40 Years

Inclusion criteria

Inclusion criteria: inclusion criteria: women aged 20-40 years old who candidate for elective or urgent cesarean section surgery. Exclusion criteria: patients with history of chronic pain; use of analgesic drugs; neurologic diseases; morbid obese patients and diabetic patients.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Paresthesia. Timepoint: Daily during 1 weak. Method of measurement: according to patient report.;Pain. Timepoint: Daily during 1 weak. Method of measurement: According to patient report.	—

Secondary

Measure	Time frame
Pain intensity, duration. Timepoint: After spinal anesthesia replenish. Method of measurement: History taking.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactParisa Golfam

Kermanshah University of Medical Sciences

pgolfam@kums.ac.ir+98 83 1725 5097

Outcome results

None listed

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