Clinical trial · Interventional
Subcutaneous Sterile Water Injection for Relief of Low Back Pain
Subcutaneous Sterile Water Injection for Relief of Low Back Pain During Normal Labor: Randomized Controlled Study
NCT02813330CI-TRIAL-00022738unknownPhase 1 / Phase 2ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
To compare the effect of subcutenous sterile water injection technique with the subcutaneous saline injection technique in the degree and duration of low back pain-relieving during childbirth
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Low Back Pain | — | UNRESOLVED | — |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| saline injection | Other | — | UNRESOLVED |
| Subcutaneous sterile water injection | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Sterile Water injection
- description
- Subcutenous injection at low back portion during labor pain
- interventionNames
- Other: Subcutaneous sterile water injection
- Other: saline injection
- type
- EXPERIMENTAL
- label
- saline injection
- description
- Subcutenous injection at low back portion during labor pain
- interventionNames
- Other: Subcutaneous sterile water injection
- Other: saline injection
Primary outcomes (2)
- measure
- Pain relief
- timeFrame
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 18 Years
- Maximum age
- 40 Years
Show eligibility criteria text
Inclusion Criteria: * In labour (spontaneous or induced record * During first stage of labour * Primary and multiparous women * A term singleton pregnancy (between 37 + 0 and 41 weeks) * Have a fetus in a cephalic presentation * Experience back pain assessed by visual analogue scale VAS and Face pain analogue * Provide informed consent. Exclusion Criteria: * Women with chronic disease * Medical condition associated with pregnancy ( Pre-eclampsia- Eclampsia- Diabetic pregnancy.... etc) * Complicated labor process ( obstructed, preterm labor, twins)
References
Publications (0)
Data not yet available
No reference posted for this study.