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NCT04883723
Effect of Manual Pressure and Shotblocker on Pain and Injection Satisfaction in Intramuscular Injection Application
NA trial testing Shotblocker in Intramuscular Injection in 120 participants. Completed in 23 August 2019.
23 August 2019
Quick facts
| Lead sponsor | TC Erciyes University |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | factorial |
| Masking | single |
| Primary purpose | prevention |
| Enrollment | 120 |
| Start date | 22 April 2019 |
| Primary completion | 23 August 2019 |
| Estimated completion | 23 August 2019 |
| Sites | 1 location across Turkey (Türkiye) |
Drugs / interventions tested
- Shotblocker — full drug profile →
- Manual Pressure
Conditions studied
- Intramuscular Injection — all drugs for Intramuscular Injection →
Sponsor
TC Erciyes University
Who can join
18 and older, any sex, with Intramuscular Injection. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
This study was planned as a single blind randomized controlled experimental study to investigate the effect of manual pressure applied before injection and ShotBlocker's pain and injection satisfaction due to intramuscular injection. The sample of the study consisted of a total of 120 patients over the age of 18 who applied to the Emergency Service of a public hospital and were requested Diclofenac Sodium 75mg / 3ml. The patients were included in the experiment I (shotblocker), experiment II (manual compression) and the control group with the randomization list created on the computer. In the ShotBlocker group, the ShotBlocker was kept throughout the injection, and in the manual compression group, manual pressure was applied to the injection area for 10 seconds before injection, and in the control group, IM injection was applied without using any tools. Before the injection, the heart rate and blood pressure values of the patient were measured and recorded. Visual Comparison Scale and Injection Satisfaction Scale were administered to the patient in the first minute after the injection. Pulse and blood pressure values were measured and recorded again. Finally, the patient introduction form was filled. Parametric or nonparametric statistical tests and correlation test were used in the analysis of the data.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT04883723
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
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Related trials
Other trials of Shotblocker
Trials testing the same drug.
- NCT07407881 — Shot Blocker and Manual Pressure Application · NA · active not recruiting
- NCT06947525 — Effects of Shotblocker and Manual Pressure on Pain and Satisfaction · NA · not yet recruiting
- NCT06646848 — Effects of Vibration, Heel Warming and Shotblocker on Pain Levels During Heel Blood Collection · NA · completed
- NCT06163027 — Effect of Shotblocker on Procedure-related Pain, Satisfaction and Comfort in Patients Receiving Spinal Anesthesia · NA · unknown
- NCT06813729 — Effects of Shotblocker® and Manual Pressure on Pain · Phase 4 · completed
Other TC Erciyes University trials
Trials by the same sponsor.
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- NCT07529964 — MMP-2/3 and Periapical Healing Outcomes · not yet recruiting
- NCT07526831 — Comparison of the Analgesic Efficacy of Adductor Canal Block and Combined Adductor Canal Block Plus IPACK Block in Knee · recruiting
- NCT07371806 — EFFETCS OF MİNDFULNESS-BASED STRESS REDUCTION İN WOMEN WİTH CORONARY ARTERY DİSEASE · NA · not yet recruiting
- NCT07499947 — Predicting Spinal Hypotension in Cesarean Section · recruiting
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT04883723 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by TC Erciyes University
- Last refreshed: 13 May 2021
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04883723.
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