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A clinical trial to compare the efficacy of pain and comfort scores for pain assessment

A randomized comparative study assessing efficacy of pain vs comfort scores

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2017/03/008248
Enrollment
180
Registered
2017-03-29
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- post caesarean section women Health Condition 2: O00-O9A- Pregnancy, childbirth and the puerperium

Interventions

None listed

Sponsors

Dayanand Medical College and Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All women who underwent caesarean section.

Exclusion criteria

Exclusion criteria: 1. Age less than 18 years 2. Deaf and dumb patients 3. Patients with intellectual disability 4. History of chronic pain or opiate abuse

Design outcomes

Primary

MeasureTime frame
Our primary outcome is to assess pain severity as measured by a 0â??10-point VNRS for pain compared with an equivalent inverted VNRS for comfort.Timepoint: between 10 to 30 hours

Secondary

MeasureTime frame
Our secondary outcomes include: 1. pain severity as measured by a VAS for pain compared with VAS for comfort; 2. whether the surgical wound is worrysome, 3. the level of worry as measured by a 0â??10-point scale, 4. whether the patient required additional analgesia; 5. whether the patient preferred to be asked about their comfort level or pain level; 6. whether the patient considered the postoperative wound to be injury and disability or healing and recovery. Timepoint: between 10 to 30 hours

Countries

India

Contacts

Public ContactRicha Jain

Dayanand Medical College and Hospital

richajain2105@gmail.com9815068242

Outcome results

None listed

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