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Comparing Recovery Pain After Laparoscopic Hysterectomy: Women With Diabetes versus Without Diabetes

Comparision of Post-operative pain using VAS and Analgesia requirement among Diabetic and Non-Diabetic patients undergoing Total Laparoscopic Hysterectomy Surgery. A Prospective Observational Study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/07/091884
Enrollment
126
Registered
2025-07-28
Start date
Unknown
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Nil: Nil Intervention2: Nil: Nil Intervention3: Nil: Nil

Sponsors

All India Institute of Medical Sciences.
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: - Patients undergoing Total Laparoscopic Hysterectomy during study period. - Age group: 40-65 years Female - ASA- I, II, III - Patients providing informed consent

Exclusion criteria

Exclusion criteria: - Patient refusal - ASA IV,V - Patients with psychiatric or neurological disorders who cannot give proper pain assessment - Patient already on multiple analgesics due to Diabetic Neuropathic Pain - Patients with kidney diseases or diagnosed diabetic nephropathy

Design outcomes

Primary

MeasureTime frame
Comparision of Pain using VAS in Diabetic and Non-Diabetic patients for 24 hours post Total Laparoscopic Hysterectomy SurgeryTimepoint: VAS assessed every 2 hourly for 24 hours post surgery.

Secondary

MeasureTime frame
Assessment of the effect of Glycosylated Haemoglobin (HbA1c) on Post-opeative Pain. Comparision of the time of first Rescue Analgesia required within 24 hrs post-operatively in Diabetic vs Non-Diabetic patients. Comparision of the frequency of Rescue Analgesia required within 24 hrs post-operatively in Diabetic vs Non-Diabetic patients. Observation of post-operative complications (if any) in 24 hours after the surgery. Assessment of Wilson sedation scale, Patient s overall satisfaction with Linkert 5 point scale Timepoint: All parameters are measured for 24 hours post-surgery.

Countries

India

Contacts

Public ContactPandya Niyati Narendrabhai

All India Institute of Medical Sciences, Rajkot.

niyatipandya9@gmail.com9427410422

Outcome results

None listed

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