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Effects of Cervical Lidocaine Spray on Pain Relief During Manual Vacuum Aspiration

Effects of Cervical Lidocaine Spray on Pain Relief During Manual Vacuum Aspiration : A Randomized Controlled Trial

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06344637
Enrollment
216
Registered
2024-04-03
Start date
2023-12-14
Completion date
2024-07-30
Last updated
2024-04-03

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

Conditions

Lidocaine, Obstetric Surgical Procedures, Pain, Procedural

Keywords

manual vacuum aspiration, pain score, Lidocaine spray

Brief summary

This randomized control trial aim to evaluate the effectiveness of local lidocaine spray application to the cervix on the reducing of pain score during the manual vacuum aspiration

Detailed description

This is a double blinded, placebo controlled study which compose of two arms. The treatment group is the local lidocaine spray application to the cervix with the intravenous opioid. The control group is the the intravenous opioid with the placebo (normal saline) before the manual vacuum aspiration. The outcome is to compare the visual analog pain score during and after procedure.

Interventions

DRUG10 % lidocaine spray without adrenaline

Pateint with indication for manual vacuum aspiration aged between 20-60 years will received a standard injection of pethidine along with 1% lidocaine spray without adrenaline on cervical os to compare pain scores with placebo. Along with measuring side effects immediately and 30 minutes after receiving 1% lidocaine without adrenaline.

OTHERPlacebo

4 puffs of normal saline apply on cervical os before manual vacuum aspiration

Sponsors

UdonThani Hospital
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Caregiver)

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* female ageed 20 years to 60 years who have an indication for manual vacuum adpiration under intraveneous analgesia

Exclusion criteria

* patient with allergic to lidocaine or history of allergic to lidocaine * patient with reproductive and urinary infection * patient with abnormal vital sign * patient with abnormal kidney and liver function test

Design outcomes

Primary

MeasureTime frameDescription
pain score during manual vauum aspirationduring surgeryThe pain score using visual analog scale is used to assess the pain score during the manual vacuum aspiration during procedure (score 0-10), the 0 score is no pain and the 10 score is the maximum pain
pain score after manual vauum aspirationat 30 minutes postoperativeThe pain score using visual analog scale is used to assess the pain score after the procedure (score 0-10) the 0 score is no pain and the 10 score is the maximum pain

Countries

Thailand

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026