Skip to content

Comparison of efficacy of modified thoracoabdominal nerve block through perichondrial approach versus oblique subcostal transversus abdominis plane block for postoperative pain management.

To compare efficacy of modified thoracoabdominal nerve block through perichondrial approach versus oblique subcostal transversus abdominis plane block for postoperative pain management. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/02/104638
Enrollment
130
Registered
2026-02-24
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: N858- Other specified noninflammatory disorders of uterus

Interventions

Intervention1: GROUP M: Patients who will receive M-TAPA block using 25ml of 0.2 percent ropivacaine.: The operator performing the block will stand on the patient s right side, with the patient posit
B. Braun Melsungen AG 34209 Melsungen, Germany) will be inserted using the in-plane technique in the caudo-cranial direction till the needle tip is placed between the transversus abdominis muscle and
B. Braun Melsungen AG 34209 Melsungen, Germany) needle will be inserted using the in-plane technique between rectus abdominis and transversus abdominis fascia. Local anaesthetic will be incrementally

Sponsors

Dayanand Medical College and Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Female patients aged 18 to 70 years scheduled for total laparoscopic hysterectomy under general anaesthesia 2. ASA I-III

Exclusion criteria

Exclusion criteria: 1. Presence of any coagulation disorder 2. Chronic opioid, alcohol or any drug abuse 3. Block injection site infection 4. Refusal to participate 5. Pregnancy 6. Allergic to local anaesthetics 7. Pre-existing cognitive dysfunction 8. BMI more than or equal to 40 kg/m

Design outcomes

Primary

MeasureTime frame
Total amount of tramadol consumed by the patient in first 24 hours postoperatively.Timepoint: Total amount of tramadol consumed by the patient in first 24 hours postoperatively.

Secondary

MeasureTime frame
1. NRS pain scores at rest & on movement. 2. Time of need for first rescue opioid analgesic. 3. Quality of patient recovery-15 score at 24 hours postoperatively. 4. Patient satisfaction using likert scale at 24 hours.Timepoint: Quality of patient recovery-15 score & patient satisfaction using likert scale at 24 hours postoperatively. NRS at 0,1,2,4,8,12 & 24 hours postoperatively.

Countries

India

Contacts

Public ContactDr Kulmeet Kaur

Dayanand Medical College and Hospital

meetmakkar893@gmail.com7009343427

Outcome results

None listed

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