Skip to content

Effect of Lidocaine Gel for Pain Relief during Endometrial Sampling in Postmenopausal bleeding: Randomized Controlled Trial

Effect of Lidocaine Gel for Pain Relief during Endometrial Sampling in Postmenopausal bleeding: Randomized Controlled Trial

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
TCTR
Registry ID
TCTR20231005003
Enrollment
72
Registered
2023-10-05
Start date
2023-03-20
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Post menopausal bleeding Post menopausal bleeding Endometrial sampling Lidocaine jelly Pain score

Interventions

2% lidocaine jelly and sterile gel 3 ml,sterile gel 3 ml
Experimental Drug,Placebo Comparator Drug
Lidocaine jelly,Placebo

Sponsors

None listed

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: women who were diagnosed with post menopausal bleeding and were literate, mature, and stable enough to do the visual analog score (VAS).

Exclusion criteria

Exclusion criteria: 1.allergy to lidocaine jelly 2.unstable vital signs for example systolic blood pressure (SBP) lower than 90 mmHg., diastolic blood pressure (SBP) lower than 60 mmHg., pulse rate more than 120 bpm., 3.patient unconsciousness or unable to answer the question and pain score.

Design outcomes

Primary

MeasureTime frame
the pain score when finishing endometrial sampling finishing endometrial sampling VAS,the pain score when finishing the procedure for 10 min when finishing the procedure for 10 min VAS,the pain score when start endometrial sampling when start endometrial sampling VAS

Secondary

MeasureTime frame
satisfied finishing the procedure for 10 min score (1-10)

Countries

Thailand

Contacts

Public ContactNathnicha Kanchana

Maharat Nakhon Ratchasima Hospital

nathnicha18@gmail.com66876916555

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026