Comparision of adition of Fentanyl and Ketamin to 5/1% lidocaine with paracervical block in reducing of post operative pain in curettage

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

IRCT

Registry ID

IRCT201305204686N7

Enrollment

120

Registered

2013-05-24

Start date

2013-03-11

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

local anaesthesia. agents primarily acting on smooth and skeletal muscles and the respiratory system

Interventions

Intervention 1: First group(40 persons) receive lidocaine 1/5% 5cc plus fentanyl 100mg. Intervention 2: Second group (40 persons) receive lidocaine 1/5% 5cc plus ketamin 50mg. Intervention 3: Third gr

Treatment - Drugs

Placebo

First group(40 persons) receive lidocaine 1/5% 5cc plus fentanyl 100mg

Second group (40 persons) receive lidocaine 1/5% 5cc plus ketamin 50mg

Third group (40 persons) lidocaine 1/5% 5cc plus placebo 2cc

Eligibility

Sex/Gender

Female

Age

20 Years to 45 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: patient candidate curettage; age 20-45 years old; informed written consent for paracervical block. Exclusion criteria: prolonged procedure >20 minutes; failure of block and need to general analgesia; allergy to analgesic substances occurring of any heart diseases.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Pain. Timepoint: 30 and 60 minutes after intervention. Method of measurement: Clinical examination.	—

Secondary

Measure	Time frame
Drug side effects. Timepoint: 30 and 60 minutes after intervention. Method of measurement: Clinical examination.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMehri Jamilian

Arak University of Medical Sciences

mjamilian@arakmu.ac.ir+98 86 1278 0660

Outcome results

None listed

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