Better pain relief after Laparoscopic hysterectomy surgery using numbing shot and paracetamol together .

The efficacy of perioperative para-cervical block with 0.25% bupivicaine as an adjuvant with intravenous paracetamol on postoperative pain relief in patients undergoing laparoscopic hysterectomy - nil

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/04/065917

Enrollment

Registered

2024-04-18

Start date

Unknown

Completion date

Unknown

Last updated

2024-04-29

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

Conditions

Health Condition 1: N920- Excessive and frequent menstruation with regular cycle

Interventions

Intervention1: Bupivicaine: 0.25%,4ml,paracervical block . Control Intervention1: patients: Age between 18 and 65 years •American Society of Anesthesiologists physical status (ASAPS) classification

Eligibility

Inclusion criteria

Inclusion criteria: 1.Age between 18 and 65 years 2.American Society of Anesthesiologists physical status (ASAPS) classification I-II 3.Planned for laparoscopic hysterectomy (includes total laparoscopic hysterectomy, laparoscopic supracervical hysterectomy, laparoscopically assisted vaginal hysterectomy, with or without salpingo-oophorectomy)

Exclusion criteria

Exclusion criteria: 1.History of cervical surgery such as conization or cerclage. 2.Inability to perform the para-cervical block due to anatomical abnormalities (i.e., very atrophicor small cervix). 3.Allergy to bupivacaine, planned concomitant surgical procedures involving extensive additional tissue manipulation such as pelvic lymph node dissection. 4.Previously taking opioids for chronic pain. 5.Chronic PID, endometriosis

Design outcomes

Primary

Measure	Time frame
To assess the efficacy of preoperative para-cervical block with 0.25% bupivacaine as an adjuvant with intravenous paracetamol on postoperative pain relief in patients undergoing laparoscopic hysterectomy.Timepoint: At 30minutes,60minutes,2hours,4hours,6hours,8hours.	—

Secondary

Measure	Time frame
To assess the efficacy of perioperative paracervical block with bupivicaine as an adjuvant with paracetamol on postoperative pain relief in patients undergoing laparoscopic hysterectomy.Timepoint: at 30minutes,60minutes,2hours,4hours,6hours,8hours.	—

Countries

India

Contacts

Public ContactPadmapriya

SrI Manakula Vinayagar Medical College and Hospital

obg.jayasreem@smvmch.ac.in9443769196

Outcome results

None listed

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