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Comparison of the effect of three methods of using localized analgesia on reducing the pain during curettage.

Comparison of the effect of three methods of using topical lidocaine gel into cervix, intrauterine infusion of lidocaine and combination of them on reducing the pain during curettage.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201707139576N3
Enrollment
120
Registered
2017-10-22
Start date
2017-03-21
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 anasthetics. Local anaesthetics

Interventions

Intervention 1: Itervention3: intrauterine Infusion of 5 cc normal saline and 3cc lidocain gel. Intervention 2: Intervention1: intrauterine Infusion of 5 cc lidocain 2% and 3cc lidocain gel. Interven
Treatment - Drugs
Itervention3: intrauterine Infusion of 5 cc normal saline and 3cc lidocain gel.
Intervention1: intrauterine Infusion of 5 cc lidocain 2% and 3cc lidocain gel.
Intervention 2: intrauterine Infusion of 5 cc lidocain 2% and 3cc placebo gel.

Sponsors

Vice-Chancellor for Research of Qazvin University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Inclusion criteria: being in the 8th-13th week of pregnancy and having a dilated cervix. Exclusion criteria: having a genital infection; suffering from severe uterine bleeding; being a drug addict; having a history of allergy to lidocaine and taking an analgesic 24 hours before curettage.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Localized analgesia. Timepoint: During localized analgesia, during curettage, 15, 30 and 60 minutes after curettage. Method of measurement: Vas pain Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAyda Zeinali

Kowsar Hospital

aydazeinali@yahoo.com+98 28 3223 6374

Outcome results

None listed

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