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Comparative evaluation of intraligamentary anesthesia and infiltration anesthesia of the maxillary nerve and its terminal branches for tooth extraction in the maxilla.

Comparative evaluation of intraligamentary anesthesia and infiltration anesthesia of the maxillary nerve and its terminal branches for tooth extraction in the maxilla.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00036055
Enrollment
30
Registered
2026-07-24
Start date
2024-12-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

K08

Interventions

Group 1: In Group A, following diagnosis, patient education, and informed consent, infiltration anesthesia was administered on the scheduled surgery day to the relevant area of the upper jaw using Ult

Sponsors

Universitätsmedizin Mainz
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Clear indication for the extraction of one or more teeth in the upper jaw

Exclusion criteria

Exclusion criteria: under 18 years non-consenting adults pregnant patients Patients with contraindications for the respective type of anesthesia (intolerances/allergies) Patients with allergies to the local anaesthetic and the stabilizer for adrenaline (sulphite) Patients with absolute contraindications to the administration of adrenaline (tachycardia, uncontrolled hyperthyroidism, pathologically increased adrenaline concentration)

Design outcomes

Primary

MeasureTime frame
Quality of effect, duration of effect and patient perception are the primary objectives of this study in a comparison of infiltration anesthesia with intraligamentary anesthesia and are assessed perioperatively, immediately postoperatively and on the first postoperative day using a Likert scale. After anesthesia has been administered, the quality of the effect is checked on the tooth or mucosa before the start of the procedure and evaluated by the patient. A new survey should be carried out immediately after the procedure. The patient's perception is assessed immediately after the end of the procedure and on the 1st day postoperatively. The questionnaire on the first postoperative day also asks about the duration of the anesthesia. The quality of the effect is assessed by ticking four different boxes with the options “complete”, “sufficient”, “incomplete” or “none”. Patients are also asked to rate the pain of the extraction on a Likert scale from 0 to 10 immediately after the procedure, with 0 meaning “no pain at all” and 10 meaning “very severe pain”. The duration of effect is noted on the documentation form during the telephone survey on the 1st day postoperatively. Patient satisfaction/patient perception is also queried during the telephone call on the 1st day postoperatively and noted using a Likert scale from 0 “not at all satisfied” to 10 “very satisfied” according to the patient.

Secondary

MeasureTime frame
Form of application, preoperatively before the start of extraction by ticking “infiltration anesthesia” or “intraligamentary anesthesia” Amount applied, postoperatively, in “ml” in the field provided field in the documentation form Post-injection, postoperative by ticking “yes” or “no” and specifying the type by ticking “infiltration” or “intraligamentary anesthesia” and specifying the quantity in “ml” in the field provided.

Countries

Germany

Contacts

Public ContactPeer Wolfgang Kämmerer

Universitätsmedizin Mainz, MKG

Peer.Kaemmerer@Unimedizin-Mainz.de06131 173752

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Aug 10, 2026