Pain relief during the procedure for taking tissue sample from inner surface of uterus

Analgesic efficacy of combined intrauterine lignocaine flushing and paracervical block in hysteroscopy guided endometrial biopsy - A randomized controlled trial - nil

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2026/02/103851

Enrollment

Registered

2026-02-13

Start date

Unknown

Completion date

Unknown

Last updated

2026-03-02

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

Conditions

Health Condition 1: - Health Condition 2: C55- Malignant neoplasm of uterus, partunspecified

Interventions

Intervention1: Paracervical block and intrauterine lignocaine flushing normal saline: intrauterine lignocaine flushing done using intrauterine insemination catheter with 2 % lignocaine Control Interve

Eligibility

Inclusion criteria

Inclusion criteria: women of repoductive age group

Exclusion criteria

Exclusion criteria: 1 Cervical stenosis 2 Cervical amputation 3 Allergy to lignocaine

Design outcomes

Primary

Measure	Time frame
To compare the analgesic efficacy of combined intrauterine lignocaine flushing and paracervical block versus paracervical block alone in women undergoing hysteroscopy guided biopsy.Timepoint: 18 months from now	—

Secondary

Measure	Time frame
1. To compare the adverse effects of combined intrauterine lignocaine flushing & paracervical block versus paracervical block alone 2. To compare patient satisfaction during & after the procedure between the two groups 3. To compare surgeon satisfaction during the procedure in the two groupsTimepoint: 18 months from now	—

Countries

India

Contacts

Public ContactDr shreen

sri manakula vinayagar medical college kalitheerthalkuppam pondicherry

poomalrpragash@gmail.com09442044679

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Mar 14, 2026